{
    "disease_id": "DOID:0080719", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011577", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011577", 
            "name": "myopathy, proximal, and ophthalmoplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011577", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011577", 
            "name": "inclusion body myopathy 3, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011577", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011577", 
            "name": "myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011577", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011577", 
            "name": "MYPOP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011577", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011577", 
            "name": "MYOPATHY, proximal, and ophthalmoplegia; MYPOP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011577", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011577", 
            "name": "inclusion body myopathy 3, autosomal dominant, formerly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080719", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080719", 
            "name": "inclusion body myopathy 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080719", 
        "description": "A myopathy that is characterized by childhood onset of congenital joint contractures, external ophthalmoplegia, and proximal muscle weakness, and that has_material_basis_in heterozygous, compound heterozygous, or homozygous mutation in the gene encoding myosin heavy chain IIa on chromosome 17p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080719", 
        "name": "proximal myopathy and ophthalmoplegia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080719#disease-associations", 
            "id": "0080719", 
            "database": "Alliance of Genome Resources"
        }
    ]
}