{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024545", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024545", 
            "name": "Miyoshi muscular dystrophy 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024545", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024545", 
            "name": "DYSF Miyoshi myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024545", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024545", 
            "name": "Miyoshi myopathy caused by mutation in DYSF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024545", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024545", 
            "name": "muscular dystrophy, distal, late-onset, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024545", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024545", 
            "name": "MIYOSHI muscular dystrophy 1; MMD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024545", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024545", 
            "name": "Miyoshi myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024545", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024545", 
            "name": "MMD1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070198", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070198", 
            "name": "Miyoshi myopathy"
        }, 
        {
            "url": "https://www.omim.org/entry/254130", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:254130", 
            "name": "Miyoshi muscular dystrophy 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070198", 
        "description": "A distal muscular dystrophy characterized by autosomal recessive inheritance of distal muscle weakness in the upper and lower limbs that spares the intrinsic muscles of the hands and has onset in young adulthood.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070198", 
        "name": "Miyoshi muscular dystrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/254130", 
            "id": "254130", 
            "database": "MIM"
        }
    ]
}