{
  "id": 13659,
  "label": "intellectual disability, autosomal recessive 12",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012612",
  "properties": {
    "xrefs": [
      "DOID:0081180",
      "GARD:0022540",
      "MEDGEN:370850",
      "MESH:C567019",
      "OMIM:611090",
      "UMLS:C1970200"
    ],
    "synonyms": [
      "intellectual developmental disorder, autosomal recessive 12",
      "intellectual disability, autosomal recessive 12",
      "intellectual disability, autosomal recessive type 12",
      "mental retardation, autosomal recessive type 12",
      "MRT12",
      "mental retardation, autosomal recessive 12"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2490",
          "ICD9:742",
          "MEDGEN:105425",
          "NCIT:C97172",
          "UMLS:C0497552"
        ],
        "synonyms": [
          "congenital abnormality of the nervous system",
          "congenital nervous system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An abnormality of the nervous system that is present at birth or detected in the neonatal period."
      },
      "child_count": 217,
      "reference_id": "MONDO:0002320"
    },
    {
      "id": 19320,
      "label": "autosomal recessive non-syndromic intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2962,
        17944,
        24319
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060308",
          "GARD:0018643",
          "MEDGEN:1826073",
          "OMIMPS:249500",
          "Orphanet:88616",
          "UMLS:C5680181"
        ],
        "synonyms": [
          "autosomal recessive intellectual disability",
          "intellectual disability, autosomal recessive",
          "AR-NSID",
          "NS-ARID",
          "autosomal recessive non-syndromic intellectual disability",
          "mental retardation, autosomal recessive",
          "non-syndromic intellectual disability, autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Autosomal recessive form of non-syndromic intellectual disability."
      },
      "child_count": 204,
      "reference_id": "MONDO:0019502"
    },
    {
      "id": 26279,
      "label": "ST3GAL3-congenital disorder of glycosylation",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17973
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "Orphanet:697734"
        ],
        "synonyms": [
          "ST3GAL3-CDG"
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0979317"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder"
    },
    {
      "id": 19320,
      "label": "autosomal recessive non-syndromic intellectual disability"
    },
    {
      "id": 26279,
      "label": "ST3GAL3-congenital disorder of glycosylation"
    }
  ]
}