{
  "id": 19054,
  "label": "non-syndromic X-linked intellectual disability",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019181",
  "properties": {
    "xrefs": [
      "DOID:0050776",
      "GARD:0018640",
      "MEDGEN:502019",
      "MESH:C564490",
      "OMIMPS:309530",
      "Orphanet:777",
      "UMLS:C3501611"
    ],
    "synonyms": [
      "X-linked non-specific intellectual disability",
      "X-linked non-syndromic intellectual disability",
      "intellectual disability, X-linked, nonsyndromic",
      "intellectual disability, nonsyndromic, X-linked",
      "mental retardation, X-linked, nonsyndromic",
      "mental retardation, nonsyndromic, X-linked",
      "non-specific X-linked intellectual disability",
      "non-syndromic X-linked intellectual disability",
      "non-syndromic intellectual disability, X-linked",
      "nonsyndromic X-linked intellectual disability",
      "isolated X-linked intellectual disability"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Nonspecific X-linked intellectual deficiencies (MRX) belong to the family of sex-linked intellectual deficiencies (XLMR). In contrast to syndromic or specific X-linked intellectual deficiencies (MRXS), which also present with associated physical, neurological and/or psychiatric manifestations, intellectual deficiency is the only symptom of MRX."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 52,
  "parents": [
    {
      "id": 2962,
      "label": "non-syndromic intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3324
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050889"
        ],
        "synonyms": [
          "isolated intellectual disability",
          "nonsyndromic intellectual disability"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An intellectual disability that is not part of a larger syndrome."
      },
      "child_count": 3,
      "reference_id": "MONDO:0000509"
    },
    {
      "id": 24021,
      "label": "X-linked intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2902,
        3324,
        24226
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:211749",
          "UMLS:C1136249"
        ],
        "synonyms": [
          "X-linked intellectual disability"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An X-linked intellectual deficiency in which not enough information is known, reported or published to indicate whether a gene causes non-syndromic or syndromic presentations."
      },
      "child_count": 6,
      "reference_id": "MONDO:0100284"
    }
  ],
  "children": [
    {
      "id": 11408,
      "label": "intellectual disability, X-linked 23",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112049",
          "GARD:0022666",
          "MEDGEN:163234",
          "MESH:C563144",
          "OMIM:300046",
          "UMLS:C0796229"
        ],
        "synonyms": [
          "MRX23",
          "intellectual disability, X-linked 23",
          "mental retardation, X-linked 23"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010230"
    },
    {
      "id": 11409,
      "label": "intellectual disability, X-linked 20",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112023",
          "GARD:0022667",
          "MEDGEN:208677",
          "MESH:C563142",
          "OMIM:300047",
          "UMLS:C0796226"
        ],
        "synonyms": [
          "MRX20",
          "intellectual disability, X-linked 20",
          "mental retardation, X-linked 20"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010231"
    },
    {
      "id": 11413,
      "label": "intellectual disability, X-linked 14",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112027",
          "GARD:0008557",
          "MEDGEN:163231",
          "MESH:C537454",
          "OMIM:300062",
          "UMLS:C0796220"
        ],
        "synonyms": [
          "MRX14",
          "intellectual disability, X-linked 14",
          "intellectual disability, X-linked nonspecific, type 14",
          "mental retardation, X-linked 14",
          "mental retardation, X-linked nonspecific, type 14"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010236"
    },
    {
      "id": 11426,
      "label": "intellectual disability, X-linked 50",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112029",
          "GARD:0022668",
          "MEDGEN:376278",
          "MESH:C564713",
          "OMIM:300115",
          "UMLS:C1848087"
        ],
        "synonyms": [
          "MRX50",
          "intellectual developmental disorder, X-linked 50",
          "intellectual disability, X-linked 50",
          "mental retardation, X-linked 50"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010251"
    },
    {
      "id": 11430,
      "label": "intellectual disability, X-linked 21",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112022",
          "GARD:0022669",
          "MEDGEN:1790509",
          "OMIM:300143",
          "UMLS:C5551510"
        ],
        "synonyms": [
          "IL1RAPL1 non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked 21, X-linked recessive",
          "intellectual disability, X-linked 21",
          "intellectual disability, X-linked type 21",
          "mental retardation, X-linked type 21",
          "non-syndromic X-linked intellectual disability caused by mutation in IL1RAPL1",
          "MRX21",
          "intellectual disability, X-linked 34",
          "mental retardation, X-linked 21",
          "mental retardation, X-linked 34"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the IL1RAPL1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010256"
    },
    {
      "id": 11440,
      "label": "intellectual disability, X-linked 58",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112024",
          "GARD:0022670",
          "MEDGEN:337526",
          "MESH:C564566",
          "OMIM:300210",
          "UMLS:C1846174"
        ],
        "synonyms": [
          "TSPAN7 non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked 58, X-linked recessive",
          "intellectual disability, X-linked 58",
          "intellectual disability, X-linked type 58",
          "mental retardation, X-linked type 58",
          "non-syndromic X-linked intellectual disability caused by mutation in TSPAN7",
          "MRX58",
          "mental retardation, X-linked 58"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the TSPAN7 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010266"
    },
    {
      "id": 11462,
      "label": "intellectual disability, X-linked 72",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112059",
          "GARD:0022671",
          "MEDGEN:375793",
          "MESH:C564547",
          "OMIM:300271",
          "UMLS:C1846038"
        ],
        "synonyms": [
          "intellectual developmental disorder, X-linked 72, X-linked recessive",
          "intellectual disability, X-linked 72",
          "intellectual disability, X-linked type 72",
          "mental retardation, X-linked type 72",
          "MRX72",
          "mental retardation, X-linked 72"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010289"
    },
    {
      "id": 11472,
      "label": "intellectual disability, X-linked 53",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112047",
          "GARD:0022672",
          "MEDGEN:335296",
          "MESH:C564533",
          "OMIM:300324",
          "UMLS:C1845889"
        ],
        "synonyms": [
          "MRX53",
          "intellectual disability, X-linked 53",
          "mental retardation, X-linked 53, X-linked recessive",
          "mental retardation, X-linked 53"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010300"
    },
    {
      "id": 11477,
      "label": "intellectual disability, X-linked 73",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112017",
          "GARD:0022673",
          "MEDGEN:335293",
          "MESH:C564528",
          "OMIM:300355",
          "UMLS:C1845860"
        ],
        "synonyms": [
          "MRX73",
          "intellectual disability, X-linked 73",
          "mental retardation, X-linked 73, X-linked recessive",
          "mental retardation, X-linked 73"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010307"
    },
    {
      "id": 11479,
      "label": "intellectual disability, X-linked 42",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112057",
          "GARD:0022674",
          "MEDGEN:337321",
          "MESH:C564524",
          "OMIM:300372",
          "UMLS:C1845810"
        ],
        "synonyms": [
          "MRX42",
          "intellectual disability, X-linked 42",
          "mental retardation, X-linked 42"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010309"
    },
    {
      "id": 11483,
      "label": "intellectual disability, X-linked 63",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112050",
          "GARD:0005613",
          "MEDGEN:337002",
          "MESH:C564522",
          "OMIM:300387",
          "UMLS:C1845672"
        ],
        "synonyms": [
          "ACSL4 non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked 63, X-linked dominant",
          "intellectual disability, X-linked 63",
          "intellectual disability, X-linked type 63",
          "mental retardation, X-linked type 63",
          "non-syndromic X-linked intellectual disability caused by mutation in ACSL4",
          "ACSL4-related intellectual disability",
          "MRX63",
          "intellectual disability, X-linked 68",
          "mental retardation, X-linked 63",
          "mental retardation, X-linked 68"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the ACSL4 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010313"
    },
    {
      "id": 11487,
      "label": "intellectual disability, X-linked, with or without seizures, ARX-related",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112021",
          "GARD:0005614",
          "MEDGEN:208681",
          "MESH:C563150",
          "MESH:C564502",
          "OMIM:300419",
          "UMLS:C0796244"
        ],
        "synonyms": [
          "ARX-related intellectual disability",
          "intellectual developmental disorder, X-linked 29, X-linked recessive",
          "intellectual disability, X-linked, with or without seizures, ARX-related",
          "MRX52",
          "MRXARX",
          "intellectual disability, X-linked 29",
          "intellectual disability, X-linked 32",
          "intellectual disability, X-linked 33",
          "intellectual disability, X-linked 38",
          "intellectual disability, X-linked 43",
          "intellectual disability, X-linked 52",
          "intellectual disability, X-linked 54",
          "intellectual disability, X-linked 76",
          "intellectual disability, X-linked 87",
          "mental retardation, X-linked 29",
          "mental retardation, X-linked 32",
          "mental retardation, X-linked 33",
          "mental retardation, X-linked 38",
          "mental retardation, X-linked 43",
          "mental retardation, X-linked 52",
          "mental retardation, X-linked 54",
          "mental retardation, X-linked 76",
          "mental retardation, X-linked 87",
          "mental retardation, X-linked, with or without seizures, ARX-RELATED",
          "mental retardation, X-linked, with or without seizures, ARX-related"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010317"
    },
    {
      "id": 11492,
      "label": "intellectual disability, X-linked 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112016",
          "GARD:0022675",
          "MEDGEN:162922",
          "MESH:C563135",
          "OMIM:300428",
          "UMLS:C0796207"
        ],
        "synonyms": [
          "MRX2",
          "intellectual disability, X-linked 2",
          "mental retardation, X-linked 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010322"
    },
    {
      "id": 11494,
      "label": "intellectual disability, X-linked 81",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112033",
          "GARD:0022676",
          "MEDGEN:335203",
          "MESH:C564515",
          "OMIM:300433",
          "UMLS:C1845531"
        ],
        "synonyms": [
          "MRX81",
          "intellectual disability, X-linked 81",
          "mental retardation, X-linked 81, X-linked recessive",
          "mental retardation, X-linked 81"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010324"
    },
    {
      "id": 11496,
      "label": "intellectual disability, X-linked 46",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112055",
          "GARD:0022677",
          "MEDGEN:337255",
          "MESH:C564513",
          "OMIM:300436",
          "UMLS:C1845526"
        ],
        "synonyms": [
          "intellectual disability, X-linked 46",
          "intellectual disability, X-linked type 46",
          "mental retardation, X-linked 46, X-linked recessive",
          "mental retardation, X-linked type 46",
          "MRX46",
          "mental retardation, X-linked 46"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010326"
    },
    {
      "id": 11499,
      "label": "intellectual disability, X-linked 77",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112039",
          "GARD:0022678",
          "MEDGEN:335199",
          "MESH:C564511",
          "OMIM:300454",
          "UMLS:C1845499"
        ],
        "synonyms": [
          "MRX77",
          "intellectual disability, X-linked 77",
          "mental retardation, X-linked 77, X-linked recessive",
          "mental retardation, X-linked 77"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010329"
    },
    {
      "id": 11513,
      "label": "intellectual disability, X-linked 45",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112028",
          "GARD:0022679",
          "MEDGEN:375633",
          "MESH:C564503",
          "OMIM:300498",
          "UMLS:C1845333"
        ],
        "synonyms": [
          "intellectual disability, X-linked 45",
          "intellectual disability, X-linked type 45",
          "mental retardation, X-linked 45",
          "mental retardation, X-linked type 45",
          "MRX45"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010344"
    },
    {
      "id": 11514,
      "label": "intellectual disability, X-linked 84",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112030",
          "GARD:0022680",
          "MEDGEN:337203",
          "MESH:C564501",
          "OMIM:300505",
          "UMLS:C1845297"
        ],
        "synonyms": [
          "MRX84",
          "intellectual disability, X-linked 84",
          "mental retardation, X-linked 84, X-linked recessive",
          "mental retardation, X-linked 84"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010347"
    },
    {
      "id": 11519,
      "label": "intellectual disability, X-linked 82",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112052",
          "GARD:0022681",
          "MEDGEN:337201",
          "MESH:C564496",
          "OMIM:300518",
          "UMLS:C1845286"
        ],
        "synonyms": [
          "MRX82",
          "intellectual disability, X-linked 82",
          "mental retardation, X-linked 82, X-linked recessive",
          "mental retardation, X-linked 82"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010352"
    },
    {
      "id": 11527,
      "label": "intellectual disability, X-linked 30",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112051",
          "GARD:0022682",
          "MEDGEN:163235",
          "OMIM:300558",
          "UMLS:C0796237"
        ],
        "synonyms": [
          "PAK3 non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked 30, X-linked recessive",
          "intellectual disability, X-linked 30",
          "intellectual disability, X-linked type 30",
          "mental retardation, X-linked type 30",
          "non-syndromic X-linked intellectual disability caused by mutation in PAK3",
          "MRX30",
          "intellectual disability, X-linked 47",
          "mental retardation, X-linked 30",
          "mental retardation, X-linked 47"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the PAK3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010361"
    },
    {
      "id": 11529,
      "label": "intellectual disability, X-linked 91",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112043",
          "GARD:0024720",
          "MEDGEN:375592",
          "MESH:C564482",
          "OMIM:300577",
          "UMLS:C1845142"
        ],
        "synonyms": [
          "intellectual disability, X-linked 91",
          "intellectual disability, X-linked type 91",
          "mental retardation, X-linked 91, X-linked dominant",
          "mental retardation, X-linked type 91",
          "MRX91",
          "mental retardation, X-linked 91"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010363"
    },
    {
      "id": 11555,
      "label": "intellectual disability, X-linked 93",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112045",
          "GARD:0024722",
          "MEDGEN:410164",
          "MESH:C567066",
          "OMIM:300659",
          "UMLS:C1970841"
        ],
        "synonyms": [
          "BRWD3 non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked 93, X-linked recessive",
          "intellectual disability, X-linked 93",
          "intellectual disability, X-linked type 93",
          "mental retardation, X-linked type 93",
          "non-syndromic X-linked intellectual disability caused by mutation in BRWD3",
          "MRX93",
          "intellectual disability, X-linked, with macrocephaly",
          "mental retardation, X-linked 93",
          "mental retardation, X-linked, with macrocephaly"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the BRWD3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010393"
    },
    {
      "id": 11567,
      "label": "chromosome Xp11.22 duplication syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DECIPHER:90",
          "DOID:0112037",
          "GARD:0022683",
          "MEDGEN:208679",
          "OMIM:300705",
          "UMLS:C0796238"
        ],
        "synonyms": [
          "Xp11.22-linked intellectual disability",
          "chromosome Xp11.22 duplication syndrome",
          "intellectual disability, X-linked 17",
          "intellectual disability, X-linked 31",
          "mental retardation, X-linked 17",
          "mental retardation, X-linked 31"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010406"
    },
    {
      "id": 11574,
      "label": "intellectual disability, X-linked 95",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022684",
          "MEDGEN:394715",
          "MESH:C567470",
          "OMIM:300716",
          "UMLS:C2678034"
        ],
        "synonyms": [
          "MRX95",
          "intellectual disability, X-linked 95",
          "mental retardation, X-linked 95, X-linked dominant",
          "mental retardation, X-linked 95"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010413"
    },
    {
      "id": 11589,
      "label": "intellectual disability, X-linked 96",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112035",
          "GARD:0022685",
          "MEDGEN:477039",
          "OMIM:300802",
          "UMLS:C3275408"
        ],
        "synonyms": [
          "SYP non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked 96, X-linked recessive",
          "intellectual disability, X-linked 96",
          "intellectual disability, X-linked type 96",
          "mental retardation, X-linked type 96",
          "non-syndromic X-linked intellectual disability caused by mutation in SYP",
          "MRX96",
          "mental retardation, X-linked 96"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the SYP gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010429"
    },
    {
      "id": 11590,
      "label": "intellectual disability, X-linked 97",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112046",
          "GARD:0022686",
          "MEDGEN:440689",
          "MESH:C567583",
          "OMIM:300803",
          "UMLS:C2749020"
        ],
        "synonyms": [
          "ZNF711 non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked 97",
          "intellectual disability, X-linked 97",
          "intellectual disability, X-linked type 97",
          "mental retardation, X-linked type 97",
          "non-syndromic X-linked intellectual disability caused by mutation in ZNF711",
          "MRX97",
          "Mrxz",
          "intellectual disability, X-linked 65",
          "mental retardation, X-linked 65",
          "mental retardation, X-linked 97"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the ZNF711 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010430"
    },
    {
      "id": 11606,
      "label": "intellectual disability, X-linked 19",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112019",
          "GARD:0022687",
          "MEDGEN:208676",
          "MESH:C563141",
          "OMIM:300844",
          "UMLS:C0796225"
        ],
        "synonyms": [
          "RPS6KA3 non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked 19, X-linked dominant",
          "intellectual disability, X-linked 19",
          "intellectual disability, X-linked type 19",
          "mental retardation, X-linked type 19",
          "non-syndromic X-linked intellectual disability caused by mutation in RPS6KA3",
          "MRX19",
          "mental retardation, X-linked 19"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the RPS6KA3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010447"
    },
    {
      "id": 11609,
      "label": "intellectual disability, X-linked 89",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112031",
          "GARD:0022688",
          "MEDGEN:333247",
          "MESH:C564036",
          "OMIM:300848",
          "UMLS:C1839082"
        ],
        "synonyms": [
          "MRX89",
          "intellectual disability, X-linked 89",
          "mental retardation, X-linked 89, X-linked dominant",
          "mental retardation, X-linked 89"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010450"
    },
    {
      "id": 11610,
      "label": "intellectual disability, X-linked 41",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112058",
          "GARD:0022689",
          "MEDGEN:854647",
          "OMIM:300849",
          "UMLS:C3887939"
        ],
        "synonyms": [
          "GDI1 non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked 41, X-linked dominant",
          "intellectual disability, X-linked 41",
          "intellectual disability, X-linked type 41",
          "mental retardation, X-linked type 41",
          "non-syndromic X-linked intellectual disability caused by mutation in GDI1",
          "MRX41",
          "intellectual disability, X-linked 48",
          "mental retardation, X-linked 41",
          "mental retardation, X-linked 48"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the GDI1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010451"
    },
    {
      "id": 11611,
      "label": "intellectual disability, X-linked 90",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112041",
          "GARD:0022690",
          "MEDGEN:477074",
          "OMIM:300850",
          "UMLS:C3275443"
        ],
        "synonyms": [
          "DLG3 non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked 90, X-linked recessive",
          "intellectual disability, X-linked 90",
          "intellectual disability, X-linked type 90",
          "mental retardation, X-linked type 90",
          "non-syndromic X-linked intellectual disability caused by mutation in DLG3",
          "MRX90",
          "mental retardation, X-linked 90"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the DLG3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010452"
    },
    {
      "id": 11612,
      "label": "intellectual disability, X-linked 92",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112032",
          "GARD:0022691",
          "MEDGEN:335109",
          "MESH:C564483",
          "OMIM:300851",
          "UMLS:C1845144"
        ],
        "synonyms": [
          "MRX92",
          "intellectual disability, X-linked 92",
          "mental retardation, X-linked 92, X-linked recessive",
          "mental retardation, X-linked 92"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010453"
    },
    {
      "id": 11613,
      "label": "intellectual disability, X-linked 88",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112053",
          "GARD:0022692",
          "MEDGEN:477075",
          "OMIM:300852",
          "UMLS:C3275444"
        ],
        "synonyms": [
          "MRX88",
          "intellectual disability, X-linked 88",
          "intellectual disability, XMEN-linked 88",
          "mental retardation, X-linked 88"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010454"
    },
    {
      "id": 11645,
      "label": "intellectual disability, X-linked 99",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112026",
          "GARD:0022693",
          "MEDGEN:813076",
          "OMIM:300919",
          "UMLS:C3806746"
        ],
        "synonyms": [
          "USP9X non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked 99, X-linked recessive",
          "intellectual disability, X-linked 99",
          "intellectual disability, X-linked type 99",
          "mental retardation, X-linked type 99",
          "non-syndromic X-linked intellectual disability caused by mutation in USP9X",
          "MRX99",
          "mental retardation, X-linked 99"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the USP9X gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010487"
    },
    {
      "id": 11646,
      "label": "intellectual disability, X-linked 100",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112040",
          "GARD:0024729",
          "MEDGEN:855516",
          "OMIM:300923",
          "UMLS:C3890167"
        ],
        "synonyms": [
          "KIF4A non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked 100, X-linked recessive",
          "intellectual disability, X-linked 100",
          "intellectual disability, X-linked type 100",
          "mental retardation, X-linked type 100",
          "non-syndromic X-linked intellectual disability caused by mutation in KIF4A",
          "MRX100",
          "mental retardation, X-linked 100"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the KIF4A gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010488"
    },
    {
      "id": 11647,
      "label": "intellectual disability, X-linked 101",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112048",
          "GARD:0022694",
          "MEDGEN:855517",
          "OMIM:300928",
          "UMLS:C3890168"
        ],
        "synonyms": [
          "MID2 non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked 101, X-linked recessive",
          "intellectual disability, X-linked 101",
          "intellectual disability, X-linked type 101",
          "mental retardation, X-linked type 101",
          "non-syndromic X-linked intellectual disability caused by mutation in MID2",
          "MRX101",
          "mental retardation, X-linked 101"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the MID2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010489"
    },
    {
      "id": 11655,
      "label": "intellectual disability, X-linked 102",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024730",
          "MEDGEN:1715418",
          "NCIT:C129931",
          "OMIM:300958",
          "UMLS:C5393299"
        ],
        "synonyms": [
          "DDX3X non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked, syndrome, Snijders Blok type, X-linked recessive, X-linked dominant",
          "intellectual disability, X-linked 102",
          "intellectual disability, X-linked type 102",
          "mental retardation, X-linked type 102",
          "non-syndromic X-linked intellectual disability caused by mutation in DDX3X",
          "DDX3X-related intellectual disability",
          "MRX102",
          "mental retardation, X-linked 102"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An inherited condition caused by mutation(s) in the DDX3X gene, encoding ATP-dependent RNA helicase DDX3X. It is characterized by severe intellectual disability and variable neurologic features."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010497"
    },
    {
      "id": 11664,
      "label": "intellectual disability, X-linked 61",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112042",
          "GARD:0022695",
          "MEDGEN:924419",
          "OMIM:300978",
          "UMLS:C4283894"
        ],
        "synonyms": [
          "MRX61",
          "RLIM non-syndromic X-linked intellectual disability",
          "Tonne-Kalscheuer syndrome",
          "intellectual disability, X-linked 61",
          "intellectual disability, X-linked type 61",
          "mental retardation, X-linked 61",
          "mental retardation, X-linked type 61",
          "non-syndromic X-linked intellectual disability caused by mutation in RLIM"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the RLIM gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010506"
    },
    {
      "id": 11666,
      "label": "intellectual disability, X-linked 103",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112020",
          "GARD:0024734",
          "MEDGEN:934785",
          "OMIM:300982",
          "UMLS:C4310818"
        ],
        "synonyms": [
          "KLHL15 non-syndromic X-linked intellectual disability",
          "MRX103",
          "intellectual developmental disorder, X-linked 103, X-linked recessive",
          "intellectual disability, X-linked 103",
          "intellectual disability, X-linked type 103",
          "mental retardation, X-linked 103",
          "mental retardation, X-linked type 103",
          "non-syndromic X-linked intellectual disability caused by mutation in KLHL15"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the KLHL15 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010508"
    },
    {
      "id": 11667,
      "label": "intellectual disability, X-linked 104",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112018",
          "GARD:0022696",
          "MEDGEN:934784",
          "OMIM:300983",
          "UMLS:C4310817"
        ],
        "synonyms": [
          "FRMPD4 non-syndromic X-linked intellectual disability",
          "MRX104",
          "intellectual developmental disorder, X-linked 104",
          "intellectual disability, X-linked 104",
          "intellectual disability, X-linked type 104",
          "mental retardation, X-linked 104",
          "mental retardation, X-linked type 104",
          "non-syndromic X-linked intellectual disability caused by mutation in FRMPD4"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the FRMPD4 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010509"
    },
    {
      "id": 11668,
      "label": "intellectual disability, X-linked 105",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112036",
          "GARD:0022697",
          "MEDGEN:934783",
          "OMIM:300984",
          "UMLS:C4310816"
        ],
        "synonyms": [
          "MRX105",
          "USP27X non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked 105, X-linked recessive",
          "intellectual disability, X-linked 105",
          "intellectual disability, X-linked type 105",
          "mental retardation, X-linked 105",
          "mental retardation, X-linked type 105",
          "non-syndromic X-linked intellectual disability caused by mutation in USP27X"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the USP27X gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010510"
    },
    {
      "id": 11802,
      "label": "intellectual disability, X-linked 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112038",
          "GARD:0022699",
          "MEDGEN:444070",
          "MESH:C564489",
          "MESH:C567906",
          "NCIT:C133729",
          "OMIM:309530",
          "Orphanet:397933",
          "UMLS:C2931498"
        ],
        "synonyms": [
          "IQSEC2-related disorder",
          "IQSEC2-related syndromic intellectual disability",
          "MRX",
          "MRX1",
          "MRX78",
          "intellectual developmental disorder, X-linked 1, X-linked dominant",
          "intellectual disability, X-linked 1",
          "mental retardation, X-linked 1",
          "mental retardation, X-linked 18",
          "mental retardation, X-linked 78",
          "mental retardation, X-linked type 1",
          "IQSEC2",
          "IQSEC2-related epilepsy",
          "IQSEC2-related intellectual disability",
          "X-linked intellectual disability 1",
          "X-linked intellectual disability 1/78",
          "X-linked intellectual disability 78",
          "severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An X-linked dominant condition caused by mutation(s) in the IQSEC2 gene, encoding IQ motif and SEC7 domain-containing protein 2. It is characterized by substantially impaired intellectual functioning and behavioral abnormalities."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010656"
    },
    {
      "id": 11803,
      "label": "methylmalonic acidemia with homocystinuria, type cblX",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17252,
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111814",
          "GARD:0013137",
          "MEDGEN:167111",
          "MESH:C563136",
          "OMIM:309541",
          "Orphanet:369962",
          "UMLS:C0796208"
        ],
        "synonyms": [
          "combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblX",
          "methylmalonic aciduria and homocysteinemia, cblx type, X-linked recessive",
          "methylmalonic aciduria with homocystinuria, type cblX",
          "intellectual disability, X-linked 3",
          "mental retardation, X-linked 3",
          "methylmalonic acidemia and HOMOCYSTEINEMIA, cblX type",
          "methylmalonic acidemia and homocysteinemia type cblX"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010657"
    },
    {
      "id": 11805,
      "label": "FRAXE intellectual disability",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080984",
          "GARD:0002378",
          "MEDGEN:155512",
          "OMIM:309548",
          "Orphanet:100973",
          "SCTID:716709002",
          "UMLS:C0751157"
        ],
        "synonyms": [
          "FRAXE intellectual disability",
          "intellectual developmental disorder, X-linked 109, X-linked recessive",
          "intellectual disability associated with fragile site FRAXE",
          "FRAXE intellectual disability syndrome",
          "FRAXE mental retardation syndrome",
          "FRAXE syndrome",
          "X-linked intellectual disability associated with fragile site FRAXE",
          "X-linked mental retardation associated with fragile site FRAXE",
          "fragile XE syndrome",
          "fragile site, folic acid type",
          "intellectual disability, X-linked, associated with fragile site FRAXE",
          "mental retardation, X-linked, associated with fragile site FRAXE"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A nonsyndromic X-linked mental retardation (NS-XLMR) characterized by mild intellectual deficit. FRAXE is the most common form of NS-XLMR."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010659"
    },
    {
      "id": 11806,
      "label": "intellectual disability, X-linked 9",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112034",
          "GARD:0022700",
          "MEDGEN:167112",
          "MESH:C563137",
          "OMIM:309549",
          "UMLS:C0796215"
        ],
        "synonyms": [
          "FTSJ1 non-syndromic X-linked intellectual disability",
          "intellectual developmental disorder, X-linked 9, X-linked recessive",
          "intellectual disability, X-linked 9",
          "intellectual disability, X-linked type 9",
          "mental retardation, X-linked type 9",
          "non-syndromic X-linked intellectual disability caused by mutation in FTSJ1",
          "MRX9",
          "intellectual disability, X-linked 44",
          "mental retardation, X-linked 44",
          "mental retardation, X-linked 9"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the FTSJ1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010660"
    },
    {
      "id": 21730,
      "label": "intellectual developmental disorder, X-linked 108",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111844",
          "GARD:0025483",
          "MEDGEN:1680544",
          "OMIM:301024",
          "UMLS:C5193009"
        ],
        "synonyms": [
          "intellectual developmental disorder, X-linked 108, X-linked recessive",
          "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 108",
          "MRX108",
          "Mental Retardation, X-Linked 108"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0026723"
    },
    {
      "id": 22112,
      "label": "intellectual disability, X-linked 106",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080240",
          "GARD:0025656",
          "MEDGEN:1389156",
          "OMIM:300997",
          "UMLS:C4478379"
        ],
        "synonyms": [
          "intellectual developmental disorder, X-linked 106, X-linked recessive",
          "intellectual disability, X-linked 106",
          "MRX106",
          "X-linked intellectual disability 106",
          "X-linked mental retardation 106",
          "mental retardation, X-linked 106"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030907"
    },
    {
      "id": 23554,
      "label": "intellectual disability, X-linked 107",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112054",
          "GARD:0022698",
          "MEDGEN:1639885",
          "OMIM:301013",
          "UMLS:C4692652"
        ],
        "synonyms": [
          "intellectual developmental disorder, X-linked 107",
          "intellectual disability, X-linked 107",
          "MRX107",
          "mental retardation, X-linked 107"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0049222"
    },
    {
      "id": 25283,
      "label": "intellectual developmental disorder, X-linked 110",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026656",
          "MEDGEN:1823954",
          "OMIM:301095",
          "UMLS:C5774180"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0859086"
    },
    {
      "id": 25603,
      "label": "intellectual developmental disorder, X-linked 111",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060929",
          "GARD:0026787",
          "MEDGEN:1840204",
          "OMIM:301107",
          "UMLS:C5829568"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0957203"
    },
    {
      "id": 25699,
      "label": "intellectual developmental disorder, X-linked 112",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026854",
          "MEDGEN:1840225",
          "OMIM:301111",
          "UMLS:C5829589"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0957496"
    },
    {
      "id": 25873,
      "label": "intellectual developmental disorder, X-linked 113",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026972",
          "MEDGEN:1852264",
          "OMIM:301116",
          "UMLS:C5882666"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0958200"
    },
    {
      "id": 26119,
      "label": "intellectual developmental disorder, X-linked 114",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027325",
          "MEDGEN:1874421",
          "OMIM:301134",
          "UMLS:C5974891"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0975828"
    }
  ],
  "roots": [
    {
      "id": 2962,
      "label": "non-syndromic intellectual disability"
    },
    {
      "id": 24021,
      "label": "X-linked intellectual disability"
    }
  ]
}