{
    "disease_id": "DOID:0111193", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008031", 
            "name": "facioscapulohumeral muscular dystrophy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008031", 
            "name": "FSHD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008031", 
            "name": "SMCHD1 facioscapulohumeral muscular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008031", 
            "name": "facioscapulohumeral muscular dystrophy 2; FSHD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008031", 
            "name": "facioscapulohumeral muscular dystrophy 2, digenic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008031", 
            "name": "muscular dystrophy, facioscapulohumeral, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008031", 
            "name": "Fshd2, digenic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008031", 
            "name": "muscular dystrophy, facioscapulohumeral, type 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008031", 
            "name": "facioscapulohumeral muscular dystrophy caused by mutation in SMCHD1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111193", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111193", 
            "name": "FSHD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111193", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111193", 
            "name": "facioscapulohumeral muscular dystrophy 1B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111193", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111193", 
            "name": "facioscapulohumeral muscular dystrophy type 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111193", 
        "description": "A facioscapulohumeral muscular dystrophy that has_material_basis_in digenic inheritance of a heterozygous mutation in SMCHDI on 18p11.32 and a haplotype on chromosome 4 that is permissive for DUX4 expression.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111193", 
        "name": "facioscapulohumeral muscular dystrophy 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/158901", 
            "id": "158901", 
            "database": "MIM"
        }
    ]
}