{
    "disease_id": "DOID:0111183",
    "recommended_name": {
        "id": "DOID:0111183",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111183",
        "name": "familial hemiplegic migraine 3",
        "description": "A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in SCN1A on 2q24.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111183",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111183",
            "name": "FHM3",
            "description": ""
        },
        {
            "id": "DOID:0111183",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111183",
            "name": "MHP3",
            "description": ""
        },
        {
            "id": "MONDO:0012320",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012320",
            "name": "migraine, familial hemiplegic, 3",
            "description": "Any familial or sporadic hemiplegic migraine in which the cause of the disease is a mutation in the SCN1A gene."
        },
        {
            "id": "MONDO:0012320",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012320",
            "name": "SCN1A familial or sporadic hemiplegic migraine",
            "description": ""
        },
        {
            "id": "MONDO:0012320",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012320",
            "name": "familial or sporadic hemiplegic migraine caused by mutation in SCN1A",
            "description": ""
        },
        {
            "id": "MONDO:0012320",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012320",
            "name": "migraine, familial hemiplegic, 3",
            "description": ""
        },
        {
            "id": "MONDO:0012320",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012320",
            "name": "migraine, familial hemiplegic, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0012320",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012320",
            "name": "FHM3",
            "description": ""
        },
        {
            "id": "MIM:609634",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/609634",
            "name": "Migraine, familial hemiplegic, 3",
            "description": "Migraine, familial hemiplegic, 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111183"
    ],
    "unlinked_id_list": []
}