{
    "disease_id": "DOID:0111181",
    "recommended_name": {
        "id": "DOID:0111181",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111181",
        "name": "familial hemiplegic migraine 1",
        "description": "A familial hemiplegic migraine that is commonly associated with cerebellar degeneration and has_material_basis_in heterozygous mutation in CACNA1A on 19p13."
    },
    "synonyms": [
        {
            "id": "DOID:0111181",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111181",
            "name": "FHM1",
            "description": ""
        },
        {
            "id": "DOID:0111181",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111181",
            "name": "MHP1",
            "description": ""
        },
        {
            "id": "DOID:0111181",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111181",
            "name": "familial hemiplegic migraine1 with progressive cerebellar ataxia",
            "description": ""
        },
        {
            "id": "MONDO:0007714",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007714",
            "name": "migraine, familial hemiplegic, 1",
            "description": "A migraine disorder characterized by an aura that includes motor weakness and the absence of family history."
        },
        {
            "id": "MONDO:0007714",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007714",
            "name": "sporadic hemiplegic migraine",
            "description": ""
        },
        {
            "id": "MONDO:0007714",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007714",
            "name": "migraine, familial hemiplegic, 1",
            "description": ""
        },
        {
            "id": "MONDO:0007714",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007714",
            "name": "FHM1",
            "description": ""
        },
        {
            "id": "MONDO:0007714",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007714",
            "name": "MHP1",
            "description": ""
        },
        {
            "id": "MONDO:0007714",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007714",
            "name": "migraine, familial hemiplegic, 1; FHM1",
            "description": ""
        },
        {
            "id": "MONDO:0007714",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007714",
            "name": "CACNA1A migraine disorder",
            "description": ""
        },
        {
            "id": "MONDO:0007714",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007714",
            "name": "migraine, familial hemiplegic, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007714",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007714",
            "name": "migraine disorder caused by mutation in CACNA1A",
            "description": ""
        },
        {
            "id": "MONDO:0007714",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007714",
            "name": "Mhp1",
            "description": ""
        },
        {
            "id": "MONDO:0007714",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007714",
            "name": "migraine, familial hemiplegic 1, with progressive cerebellar ataxia",
            "description": ""
        },
        {
            "id": "MONDO:0007714",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007714",
            "name": "familial hemiplegic migraine type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007714",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007714",
            "name": "Fhm",
            "description": ""
        },
        {
            "id": "MONDO:0007714",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007714",
            "name": "migraine, sporadic hemiplegic",
            "description": ""
        },
        {
            "id": "MONDO:0007714",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007714",
            "name": "hemiplegic migraine, familial type 1",
            "description": ""
        },
        {
            "id": "MIM:141500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/141500",
            "name": "Migraine, familial hemiplegic, 1",
            "description": "Migraine, familial hemiplegic, 1"
        }
    ]
}