{
    "disease_id": "DOID:0110266", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011413", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011413", 
            "name": "cataract 9, multiple types"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011413", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011413", 
            "name": "CATC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011413", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011413", 
            "name": "cataract 9, multiple types, with or without microcornea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011413", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011413", 
            "name": "CTRCT9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011413", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011413", 
            "name": "cataract, autosomal recessive congenital 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011413", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011413", 
            "name": "CRYAA cataract (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011413", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011413", 
            "name": "cataract, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011413", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011413", 
            "name": "cataract 9 multiple types with or without microcornea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011413", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011413", 
            "name": "cataract 9, multiple types; CTRCT9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011413", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011413", 
            "name": "cataract (disease) caused by mutation in CRYAA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011413", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011413", 
            "name": "autosomal recessive congenital cataract 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110266", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110266", 
            "name": "cataract 9 multiple types with or without microcornea"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110266", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110266", 
            "name": "CTRCT9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110266", 
        "description": "A cataract that has_material_basis_in autosomal recessive or autosomal dominant inheritance of heterozygous or homozygous mutation in the CRYAA gene, which encodes alpha-A-crystallin, on chromosome 21q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110266", 
        "name": "cataract 9 multiple types"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110266#disease-associations", 
            "id": "0110266", 
            "database": "Alliance of Genome Resources"
        }
    ]
}