{
  "id": 12352,
  "label": "migraine, familial hemiplegic, 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011232",
  "properties": {
    "xrefs": [
      "DOID:0111182",
      "GARD:0010095",
      "MEDGEN:355962",
      "MESH:C537246",
      "OMIM:602481",
      "UMLS:C1865322"
    ],
    "synonyms": [
      "ATP1A2 familial or sporadic hemiplegic migraine",
      "familial or sporadic hemiplegic migraine caused by mutation in ATP1A2",
      "migraine, familial hemiplegic, 2",
      "migraine, familial hemiplegic, type 2",
      "FHM2",
      "Mhp2",
      "familial hemiplegic migraine type 2",
      "hemiplegic migraine, familial type 2",
      "migraine, familial basilar"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any familial or sporadic hemiplegic migraine in which the cause of the disease is a mutation in the ATP1A2 gene."
  },
  "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3089,
      "label": "familial hemiplegic migraine"
    }
  ]
}