{
    "disease_id": "DOID:0060255", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019947", 
            "name": "rippling muscle disease 2; RMD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019947", 
            "name": "muscular dystrophy limb-girdle type IC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019947", 
            "name": "rippling muscle disease caused by mutation in CAV3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019947", 
            "name": "muscular dystrophy, limb-girdle, type 1C; LGMD1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019947", 
            "name": "rippling muscle disease type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019947", 
            "name": "limb-girdle muscular dystrophy type 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019947", 
            "name": "autosomal dominant limb-girdle muscular dystrophy caused by mutation in CAV3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019947", 
            "name": "LGMD1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019947", 
            "name": "limb-girdle muscular dystrophy due to caveolin-3 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019947", 
            "name": "muscular dystrophy, limb-girdle, type IC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019947", 
            "name": "CAV3 autosomal dominant limb-girdle muscular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019947", 
            "name": "RMD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019947", 
            "name": "muscular dystrophy, limb-girdle, type 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019947", 
            "name": "CAV3 rippling muscle disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060255", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060255", 
            "name": "autosomal dominant limb-girdle muscular dystrophy type 1C"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060255", 
        "description": "A muscle tissue disease characterized by mechanically triggered contractions of skeletal muscle and that has_material_basis_in mutation in the caveolin-3 gene (CAV3) on chromosome 3p25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060255", 
        "name": "rippling muscle disease 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060255#disease-associations", 
            "id": "0060255", 
            "database": "Alliance of Genome Resources"
        }
    ]
}