{
    "disease_id": "DOID:0080093", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012130", 
            "name": "alpha-B crystallinopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012130", 
            "name": "myopathy, desmin-related, associated with mutation in the Cryab Gene"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012130", 
            "name": "alpha-B crystallin-related late-onset distal myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012130", 
            "name": "myopathy, myofibrillar, alpha-B crystallin-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012130", 
            "name": "myofibrillar myopathy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012130", 
            "name": "myopathy, myofibrillar, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012130", 
            "name": "myopathy, myofibrillar, with or without cataract and/or cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012130", 
            "name": "myopathy, myofibrillar, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012130", 
            "name": "late-onset distal crystallinopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012130", 
            "name": "autosomal dominant distal myopathy caused by mutation in CRYAB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012130", 
            "name": "CRYAB autosomal dominant distal myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012130", 
            "name": "myopathy, myofibrillar, 2; MFM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012130", 
            "name": "MFM2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080093", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080093", 
            "name": "alpha-b crystallinopathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080093", 
        "description": "A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the alpha-B-crystallin gene on chromosome 11q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080093", 
        "name": "myofibrillar myopathy 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080093#disease-associations", 
            "id": "0080093", 
            "database": "Alliance of Genome Resources"
        }
    ]
}