{
    "disease_id": "DOID:0070097",
    "recommended_name": {
        "id": "DOID:0070097",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070097",
        "name": "oculocutaneous albinism type III",
        "description": "An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the TYRP1 gene on chromosome 9p23."
    },
    "synonyms": [
        {
            "id": "DOID:0070097",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070097",
            "name": "OCA3",
            "description": ""
        },
        {
            "id": "DOID:0070097",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070097",
            "name": "Rufous Oculocutaneous Albinism",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "oculocutaneous albinism type 3",
            "description": "Type 3 oculocutaneous albinism (OCA3) is a form of oculocutaneous albinism (OCA) characterized by rufous or brown albinism and occurring mainly in the African population."
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "OCA3",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "Red oculocutaneous albinism",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "TYRP1 oculocutaneous albinism",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "oculocutaneous albinism caused by mutation in TYRP1",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "oculocutaneous albinism type 3",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "rufous oculocutaneous albinism",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "xanthous oculocutaneous albinism",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "ROCA",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "Xanthism",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "albinism 3",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "albinism, oculocutaneous, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "albinism, oculocutaneous, type III",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "oculocutaneous albinism type III",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "oculocutaneous albinism, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "rufous OCA",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "oculocutaneous albinism type 3",
            "description": "Type 3 oculocutaneous albinism (OCA3) is a form of oculocutaneous albinism (OCA) characterized by rufous or brown albinism and occurring mainly in the African population."
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "OCA3",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "Red oculocutaneous albinism",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "TYRP1 oculocutaneous albinism",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "oculocutaneous albinism caused by mutation in TYRP1",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "oculocutaneous albinism type 3",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "rufous oculocutaneous albinism",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "xanthous oculocutaneous albinism",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "ROCA",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "Xanthism",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "albinism 3",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "albinism, oculocutaneous, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "albinism, oculocutaneous, type III",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "oculocutaneous albinism type III",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "oculocutaneous albinism, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0008747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008747",
            "name": "rufous OCA",
            "description": ""
        },
        {
            "id": "MIM:203290",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/203290",
            "name": "Albinism, oculocutaneous, 3",
            "description": "Albinism, oculocutaneous, 3"
        }
    ]
}