{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013484", 
            "name": "cataract type 36"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013484", 
            "name": "cataract 36; CTRCT36"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013484", 
            "name": "cataract (disease) caused by mutation in TDRD7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013484", 
            "name": "cataract, autosomal recessive congenital 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013484", 
            "name": "autosomal recessive congenital cataract 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013484", 
            "name": "TDRD7 cataract (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013484", 
            "name": "CATC4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013484", 
            "name": "CTRCT36"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110247", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110247", 
            "name": "CATC4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110247", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110247", 
            "name": "CTRCT36"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110247", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110247", 
            "name": "autosomal recessive congenital cataract 4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110247", 
        "description": "A cataract that has_material_basis_in homozygous mutation in the TDRD7 gene on chromosome 9q22.33.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110247", 
        "name": "cataract 36"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613887", 
            "id": "613887", 
            "database": "MIM"
        }
    ]
}