{
    "disease_id": "DOID:0050633", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021019", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021019", 
            "name": "X-linked recessive ocular albinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021019", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021019", 
            "name": "albinism, ocular, type I; OA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021019", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021019", 
            "name": "ocular albinism type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021019", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021019", 
            "name": "OA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021019", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021019", 
            "name": "X-linked ocular albinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021019", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021019", 
            "name": "albinism, ocular, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021019", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021019", 
            "name": "albinism, ocular, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021019", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021019", 
            "name": "Nettleship-Falls syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021019", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021019", 
            "name": "XLOA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021019", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021019", 
            "name": "ocular albinism, Nettleship-Falls type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021019", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021019", 
            "name": "Nettleship-Falls type ocular albinism"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050633", 
        "description": "An eye disease that is characterized by reduced pigmentation of the iris and the resulting impairment of visual acuity without significantly affecting the color of skin or hair and has_material_basis in mutation in the GPR143 gene that encodes segments of the melanosomes that stores melanin.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050633", 
        "name": "ocular albinism"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050633#disease-associations", 
            "id": "0050633", 
            "database": "Alliance of Genome Resources"
        }
    ]
}