{
    "disease_id": "DOID:0111182",
    "recommended_name": {
        "id": "DOID:0111182",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111182",
        "name": "familial hemiplegic migraine 2",
        "description": "A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in ATP1A2 on 1q23.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111182",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111182",
            "name": "FHM2",
            "description": ""
        },
        {
            "id": "DOID:0111182",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111182",
            "name": "Familial hemiplegic migraine-2",
            "description": ""
        },
        {
            "id": "DOID:0111182",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111182",
            "name": "MHP2",
            "description": ""
        },
        {
            "id": "MONDO:0011232",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011232",
            "name": "migraine, familial hemiplegic, 2",
            "description": "Any familial or sporadic hemiplegic migraine in which the cause of the disease is a mutation in the ATP1A2 gene."
        },
        {
            "id": "MONDO:0011232",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011232",
            "name": "hemiplegic migraine, familial type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011232",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011232",
            "name": "migraine, familial hemiplegic, 2; FHM2",
            "description": ""
        },
        {
            "id": "MONDO:0011232",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011232",
            "name": "FHM2",
            "description": ""
        },
        {
            "id": "MONDO:0011232",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011232",
            "name": "migraine, familial basilar",
            "description": ""
        },
        {
            "id": "MONDO:0011232",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011232",
            "name": "migraine, familial hemiplegic, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011232",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011232",
            "name": "familial or sporadic hemiplegic migraine caused by mutation in ATP1A2",
            "description": ""
        },
        {
            "id": "MONDO:0011232",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011232",
            "name": "Mhp2",
            "description": ""
        },
        {
            "id": "MONDO:0011232",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011232",
            "name": "familial hemiplegic migraine type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011232",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011232",
            "name": "migraine, familial hemiplegic, 2",
            "description": ""
        },
        {
            "id": "MONDO:0011232",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011232",
            "name": "ATP1A2 familial or sporadic hemiplegic migraine",
            "description": ""
        },
        {
            "id": "MIM:602481",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/602481",
            "name": "Migraine, familial hemiplegic, 2",
            "description": "Migraine, familial hemiplegic, 2"
        }
    ]
}