{
  "id": 23793,
  "label": "FOXG1 disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100040",
  "properties": {
    "xrefs": [
      "DOID:0070657",
      "GARD:0026022",
      "ICD10CM:F84.8",
      "MEDGEN:462055",
      "NCIT:C176903",
      "OMIM:613454",
      "Orphanet:561854",
      "Orphanet:598164",
      "UMLS:C3150705"
    ],
    "synonyms": [
      "FOXG1 disorder",
      "FOXG1 inherited genetic disease",
      "FOXG1 syndrome",
      "FOXG1 syndrome due to intragenic alteration",
      "FOXG1-related epileptic-dyskinetic encephalopathy",
      "Rett syndrome, congenital variant",
      "inherited genetic disease caused by mutation in FOXG1"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A monogenic disease that has material basis in mutation in the FOXG1 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3009,
      "label": "pervasive developmental disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7159,
        23791
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060040",
          "GARD:0027041",
          "ICD9:299.80",
          "MEDGEN:99336",
          "MESH:D002659",
          "NCIT:C97179",
          "SCTID:35919005",
          "UMLS:C0524528"
        ],
        "synonyms": [
          "pervasive child development disorders",
          "pervasive development disorders"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A category of developmental disorders characterized by impaired communication and socialization skills. The impairments are incongruent with the individual's developmental level or mental age. These disorders can be associated with general medical or genetic conditions."
      },
      "child_count": 10,
      "reference_id": "MONDO:0000594"
    },
    {
      "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": 17975,
      "label": "atypical Rett syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24488
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0004694",
          "MEDGEN:440664",
          "NANDO:1200605",
          "Orphanet:3095",
          "SCTID:718393002",
          "UMLS:C2748910",
          "icd11.foundation:605088126"
        ],
        "synonyms": [
          "Rett syndrome variant",
          "atypical RTT",
          "Rett like syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neurodevelopmental disorder that is diagnosed when a child presents with a Rett-like syndrome but does not fulfill all the diagnostic criteria for typical Rett syndrome (classic/typical RTT)."
      },
      "child_count": 2,
      "reference_id": "MONDO:0017746"
    },
    {
      "id": 24226,
      "label": "Mendelian neurodevelopmental disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24270,
        24488
      ],
      "type_id": 0,
      "properties": {
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neurodevelopmental disorder that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 550,
      "reference_id": "MONDO:0100500"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3009,
      "label": "pervasive developmental disorder"
    },
    {
      "id": 4427,
      "label": "congenital nervous system disorder"
    },
    {
      "id": 17975,
      "label": "atypical Rett syndrome"
    },
    {
      "id": 24226,
      "label": "Mendelian neurodevelopmental disorder"
    }
  ]
}