{
  "id": 18517,
  "label": "bilirubin encephalopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018477",
  "properties": {
    "xrefs": [
      "DOID:2382",
      "GARD:0006830",
      "ICD10CM:P57",
      "MEDGEN:44018",
      "MESH:D007647",
      "MedDRA:10023376",
      "NCIT:C84799",
      "Orphanet:415286",
      "SCTID:50143004",
      "UMLS:C0022610"
    ],
    "synonyms": [
      "bilirubin encephalopathy",
      "kernicterus",
      "hyperbilirubinemic encephalopathy",
      "kernicterus spectrum disorder"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 7209,
      "label": "brain disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4657
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:936",
          "EFO:0005774",
          "ICD9:348.3",
          "ICD9:348.30",
          "ICD9:348.8",
          "ICD9:348.9",
          "MEDGEN:14214",
          "MESH:D001927",
          "NCIT:C96413",
          "SCTID:81308009",
          "UMLS:C0006111"
        ],
        "synonyms": [
          "brain disease",
          "brain disease or disorder",
          "disease of brain",
          "disease or disorder of brain",
          "disorder of brain",
          "encephalopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A disease affecting the brain or part of the brain."
      },
      "child_count": 71,
      "reference_id": "MONDO:0005560"
    },
    {
      "id": 17982,
      "label": "inborn disorder of bilirubin metabolism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17981,
        21409
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021347",
          "MEDGEN:1671515",
          "Orphanet:309816",
          "UMLS:C0349427",
          "icd11.foundation:1297666279"
        ],
        "synonyms": [
          "disorder of bilirubin metabolism",
          "disorder of bilirubin metabolism and excretion",
          "hereditary bilirubin metabolism disease",
          "inborn disorder of bilirubin metabolism and excretion",
          "bilirubin metabolism disorder"
        ],
        "definition": "An instance of bilirubin metabolism disease that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 10,
      "reference_id": "MONDO:0017755"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [
    {
      "id": 8048,
      "label": "kernicterus due to isoimmunization",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3480,
        18517
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12043",
          "GARD:0024440",
          "ICD10CM:P57.0",
          "ICD9:773.4",
          "MEDGEN:542597",
          "NCIT:C101270",
          "SCTID:359007",
          "UMLS:C0270204",
          "icd11.foundation:1111245443"
        ],
        "synonyms": [
          "kernicterus - due to isoimm.",
          "kernicterus due to isoimmunization of fetus or newborn",
          "kernicterus due to isoimmunization of foetus or newborn",
          "kernicterus related to isoimmunization"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Encephalopathy in infants due to high levels of unconjugated bilirubin that are a result of Rh incompatibility between the mother and the fetus."
      },
      "child_count": 0,
      "reference_id": "MONDO:0006567"
    }
  ],
  "roots": [
    {
      "id": 7209,
      "label": "brain disorder"
    },
    {
      "id": 17982,
      "label": "inborn disorder of bilirubin metabolism"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}