{
    "disease_id": "DOID:0070094", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008745", 
            "name": "oculocutaneous albinism type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008745", 
            "name": "TYR oculocutaneous albinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008745", 
            "name": "oculocutaneous albinism, tyrosinase-negative"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008745", 
            "name": "albinism 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008745", 
            "name": "OCA1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008745", 
            "name": "albinism, oculocutaneous, type IA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008745", 
            "name": "tyrosinase-negative oculocutaneous albinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008745", 
            "name": "albinism, oculocutaneous, type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008745", 
            "name": "oculocutaneous albinism, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008745", 
            "name": "oculocutaneous albinism caused by mutation in TYR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008745", 
            "name": "albinism, oculocutaneous, type IA; OCA1A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070094", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070094", 
            "name": "OCA1A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070094", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070094", 
            "name": "Oculocutaneous Albinism, Tyrosinase-Negative"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070094", 
        "description": "An oculocutaneous albinism that has_material_basis_in an autosomal recessive null mutation of TYR on chromosome 11q14.3 with no residual protein activity.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070094", 
        "name": "oculocutaneous albinism type IA"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070094#disease-associations", 
            "id": "0070094", 
            "database": "Alliance of Genome Resources"
        }
    ]
}