{
    "disease_id": "DOID:0080102", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009711", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009711", 
            "name": "congenital fiber-type disproportion myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009711", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009711", 
            "name": "myopathy, congenital, with fiber-type disproportion; CFTD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009711", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009711", 
            "name": "CFTDM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009711", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009711", 
            "name": "myopathy, congenital with fiber-type disproportion"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009711", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009711", 
            "name": "fiber-type disproportion myopathy, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009711", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009711", 
            "name": "congenital fiber type disproportion"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009711", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009711", 
            "name": "CFTD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009711", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009711", 
            "name": "myopathy, congenital, with fiber-type disproportion"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080102", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080102", 
            "name": "CFTD"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080102", 
        "description": "A congenital myopathy that is characterized by skeletal muscle weakness, particularly in the muscles of the shoulders, upper arms, hips, and thighs.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080102", 
        "name": "congenital fiber-type disproportion"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080102#disease-associations", 
            "id": "0080102", 
            "database": "Alliance of Genome Resources"
        }
    ]
}