{
    "disease_id": "DOID:0070197", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008050", 
            "name": "Laing early-onset distal myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008050", 
            "name": "MPD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008050", 
            "name": "myopathy, late distal hereditary"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008050", 
            "name": "myopathy, distal, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008050", 
            "name": "Gowers disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008050", 
            "name": "myopathy, distal, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008050", 
            "name": "Laing distal myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008050", 
            "name": "myopathy, distal, 1; MPD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008050", 
            "name": "distal myopathy type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008050", 
            "name": "myopathy, distal, early-onset, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008050", 
            "name": "myopathy distal, type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070197", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070197", 
            "name": "Distal myopathy type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070197", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070197", 
            "name": "Gowers disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070197", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070197", 
            "name": "Laing distal myopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070197", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070197", 
            "name": "Laing early-onset distal myopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070197", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070197", 
            "name": "MPD1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070197", 
        "description": "A distal muscular dystrophy characterized by autosomal dominant inheritance that has_material_basis_in mutation in the MYH7 gene on chromosome 14q11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070197", 
        "name": "distal myopathy 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070197#disease-associations", 
            "id": "0070197", 
            "database": "Alliance of Genome Resources"
        }
    ]
}