{
    "disease_id": "DOID:0111192",
    "recommended_name": {
        "id": "DOID:0111192",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111192",
        "name": "facioscapulohumeral muscular dystrophy 1",
        "description": "A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35."
    },
    "synonyms": [
        {
            "id": "DOID:0111192",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111192",
            "name": "FSHD1",
            "description": ""
        },
        {
            "id": "DOID:0111192",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111192",
            "name": "facioscapulohumeral muscular dystrophy type 1",
            "description": ""
        },
        {
            "id": "DOID:0111192",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111192",
            "name": "facioscapulohumeral muscular dystrophy type 1A",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "facioscapulohumeral muscular dystrophy 1",
            "description": "Any facioscapulohumeral muscular dystrophy in which the cause of the disease is a mutation in the FRG1 gene."
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "FMD",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "FSHD",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "facioscapulohumeral muscular dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "FRG1 facioscapulohumeral muscular dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "facioscapulohumeral muscular dystrophy 1",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "facioscapulohumeral muscular dystrophy caused by mutation in FRG1",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "facioscapulohumeral muscular dystrophy type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "muscular dystrophy, facioscapulohumeral, type 1A",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "FSHD1",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "FSHD1A",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "FSHMD1A",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "Landouzy-Dejerine muscular dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "Landouzy-Dejerine muscular dystrophy facioscapulohumeral muscular dystrophy, infantile, included",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles, included",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "facioscapulohumeral muscular dystrophy 1A",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "facioscapulohumeral muscular dystrophy, infantile",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "muscular dystrophy, facioscapulohumeral",
            "description": ""
        },
        {
            "id": "MONDO:0008030",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008030",
            "name": "muscular dystrophy, facioscapulohumeral, type 1",
            "description": ""
        },
        {
            "id": "MIM:158900",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/158900",
            "name": "Facioscapulohumeral muscular dystrophy 1",
            "description": "Facioscapulohumeral muscular dystrophy 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111192"
    ],
    "unlinked_id_list": []
}