{
    "disease_id": "DOID:0111182", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011232", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011232", 
            "name": "migraine, familial hemiplegic, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011232", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011232", 
            "name": "hemiplegic migraine, familial type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011232", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011232", 
            "name": "migraine, familial hemiplegic, 2; FHM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011232", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011232", 
            "name": "FHM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011232", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011232", 
            "name": "migraine, familial basilar"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011232", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011232", 
            "name": "migraine, familial hemiplegic, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011232", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011232", 
            "name": "familial or sporadic hemiplegic migraine caused by mutation in ATP1A2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011232", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011232", 
            "name": "Mhp2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011232", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011232", 
            "name": "familial hemiplegic migraine type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011232", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011232", 
            "name": "ATP1A2 familial or sporadic hemiplegic migraine"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111182", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111182", 
            "name": "FHM2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111182", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111182", 
            "name": "Familial hemiplegic migraine-2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111182", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111182", 
            "name": "MHP2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111182", 
        "description": "A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in ATP1A2 on 1q23.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111182", 
        "name": "familial hemiplegic migraine 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111182#disease-associations", 
            "id": "0111182", 
            "database": "Alliance of Genome Resources"
        }
    ]
}