{
    "disease_id": "DOID:0070097", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008747", 
            "name": "oculocutaneous albinism type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008747", 
            "name": "rufous oculocutaneous albinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008747", 
            "name": "OCA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008747", 
            "name": "albinism, oculocutaneous, type III; OCA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008747", 
            "name": "Xanthism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008747", 
            "name": "albinism, oculocutaneous, type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008747", 
            "name": "TYRP1 oculocutaneous albinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008747", 
            "name": "albinism, oculocutaneous, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008747", 
            "name": "ROCA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008747", 
            "name": "albinism 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008747", 
            "name": "xanthous oculocutaneous albinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008747", 
            "name": "oculocutaneous albinism caused by mutation in TYRP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008747", 
            "name": "rufous OCA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008747", 
            "name": "Red oculocutaneous albinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008747", 
            "name": "oculocutaneous albinism, type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070097", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070097", 
            "name": "OCA3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070097", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070097", 
            "name": "Rufous Oculocutaneous Albinism"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070097", 
        "description": "An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of TYRP1 on chromosome 9p23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070097", 
        "name": "oculocutaneous albinism type III"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070097#disease-associations", 
            "id": "0070097", 
            "database": "Alliance of Genome Resources"
        }
    ]
}