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