{
  "id": 20158,
  "label": "migraine, familial hemiplegic, 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020756",
  "properties": {
    "xrefs": [
      "DOID:0111181",
      "GARD:0002638",
      "MEDGEN:331388",
      "MESH:C536890",
      "OMIM:141500",
      "UMLS:C1832884",
      "icd11.foundation:1583236457"
    ],
    "synonyms": [
      "FHM1",
      "MHP1",
      "familial hemiplegic migraine type 1",
      "hemiplegic migraine, familial type 1",
      "migraine, familial hemiplegic 1, with progressive cerebellar ataxia",
      "migraine, familial hemiplegic, 1",
      "migraine, familial hemiplegic, 1, with progressive cerebellar ataxia",
      "migraine, familial hemiplegic, type 1",
      "migraine, sporadic hemiplegic"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3089,
      "label": "familial hemiplegic migraine",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18849,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060178",
          "GARD:0010975",
          "ICD9:346.8",
          "MEDGEN:87374",
          "NCIT:C117009",
          "OMIMPS:141500",
          "SCTID:95656000",
          "UMLS:C0338484",
          "icd11.foundation:1827007904"
        ],
        "synonyms": [
          "FHM",
          "familial hemiplegic migraine",
          "hereditary hemiplegic migraine",
          "hemiplegic migraine, familial",
          "hemiplegic-ophthalmoplegic migraine"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A migraine disorder characterized by individual and family history of aura that includes motor weakness."
      },
      "child_count": 10,
      "reference_id": "MONDO:0000700"
    },
    {
      "id": 23992,
      "label": "CACNA1A-related complex neurodevelopmental disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24226,
        24241
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027064"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A progressive complex neurodevelopmental condition caused by variants in the CACNA1A gene. Phenotypic onset (usually) occurs around age 1 and most often includes intellectual disability but can also include epileptic encephalopathy, benign paroxysmal torticollis of infancy and paroxysmal tonic upgaze psychomotor delay, learning difficulties, absence epilepsy, episodic ataxia, and hemiplegic migraines."
      },
      "child_count": 8,
      "reference_id": "MONDO:0100254"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3089,
      "label": "familial hemiplegic migraine"
    },
    {
      "id": 23992,
      "label": "CACNA1A-related complex neurodevelopmental disorder"
    }
  ]
}