{
  "id": 19945,
  "label": "subcortical band heterotopia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020491",
  "properties": {
    "xrefs": [
      "DOID:0111169",
      "GARD:0001904",
      "MEDGEN:336288",
      "NANDO:1201070",
      "NCIT:C116933",
      "Orphanet:99796",
      "UMLS:C1848201",
      "icd11.foundation:525786944"
    ],
    "synonyms": [
      "double cortex syndrome",
      "subcortical laminar heterotopia",
      "Double cortex",
      "familial band heterotopia"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A developmental brain abnormality characterized by atypical migration of neurons during cortical development."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "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"
    }
  ],
  "children": [
    {
      "id": 11416,
      "label": "lissencephaly type 1 due to doublecortin gene mutation",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16079,
        19945
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112239",
          "GARD:0006914",
          "MEDGEN:1644310",
          "OMIM:300067",
          "Orphanet:2148",
          "SCTID:715780008",
          "UMLS:C4551968",
          "icd11.foundation:891064255"
        ],
        "synonyms": [
          "X-linked lissencephaly type 1",
          "lissencephaly type 1 due to doublecortin gene mutation",
          "lissencephaly, X-linked",
          "lissencephaly, X-linked, type 1",
          "subcortical laminal heterotopia, X-linked",
          "Dc syndrome",
          "Double cortex syndrome",
          "LISX",
          "LISX1",
          "X-linked lissencephaly",
          "XLIS",
          "Xlis",
          "lissencephaly X-linked",
          "lissencephaly and agenesis of corpus callosum",
          "lissencephaly, X-linked, 1",
          "subcortical band heterotopia, X-linked",
          "subcortical laminar heterotopia, X-linked",
          "subcortical laminar heterotopia, X-linked,"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Type 1 lissencephaly due to doublecortin (DCX) gene mutations is a semi-dominant X-linked disease characterized by intellectual deficiency and seizures that are more severe in male patients."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010239"
    },
    {
      "id": 12007,
      "label": "band heterotopia of brain",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19945,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0002250",
          "MEDGEN:924885",
          "MESH:C563950",
          "OMIM:600348",
          "UMLS:C4284594"
        ],
        "synonyms": [
          "band heterotopia of brain",
          "BH",
          "band heterotopia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010873"
    }
  ],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 4427,
      "label": "congenital nervous system disorder"
    }
  ]
}