{
    "disease_id": "DOID:0110639", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013177", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013177", 
            "name": "congenital muscular dystrophy caused by mutation in ITGA7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013177", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013177", 
            "name": "muscular dystrophy, congenital, due to integrin ALPHA-7 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013177", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013177", 
            "name": "congenital muscular dystrophy with integrin alpha-7 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013177", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013177", 
            "name": "congenital muscular dystrophy with ITGA7 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013177", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013177", 
            "name": "congenital myopathy due to integrin alpha-7 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013177", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013177", 
            "name": "muscular dystrophy, congenital, due to ITGA7 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013177", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013177", 
            "name": "ITGA7 congenital muscular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013177", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013177", 
            "name": "myopathy, congenital, due to integrin Alpha-7 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110639", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110639", 
            "name": "congenital myopathy due to integrin alpha-7 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110639", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110639", 
            "name": "congenital muscular dystrophy with ITGA7 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110639", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110639", 
            "name": "congenital muscular dystrophy with integrin alpha-7 deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/613204", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613204", 
            "name": "Muscular dystrophy congenital due to integrin alpha-7 deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110639", 
        "description": "A congenital muscular dystrophy characterized by autosomal recessive inheritance that has_material_basis_in compound heterozygous mutation in the ITGA7 gene on chromosome 12q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110639", 
        "name": "congenital muscular dystrophy due to integrin alpha-7 deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613204", 
            "id": "613204", 
            "database": "MIM"
        }
    ]
}