{
    "disease_id": "DOID:0070096",
    "recommended_name": {
        "id": "DOID:0070096",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070096",
        "name": "oculocutaneous albinism type II",
        "description": "An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of OCA2 on chromosome 15q12-q13."
    },
    "synonyms": [
        {
            "id": "DOID:0070096",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070096",
            "name": "OCA2",
            "description": ""
        },
        {
            "id": "DOID:0070096",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070096",
            "name": "Oculocutaneous Albinism, Tyrosinase-Positive",
            "description": ""
        },
        {
            "id": "MONDO:0008746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008746",
            "name": "oculocutaneous albinism type 2",
            "description": "Oculocutaneous albinism type 2 (OCA2) is a type of OCA (see this term) and the most common form of OCA seen in the African population, characterized by variable hypopigmentation of the skin and hair, numerous characteristic ocular changes and misrouting of the optic nerves at the chiasm."
        },
        {
            "id": "MONDO:0008746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008746",
            "name": "Brown oculocutaneous albinism",
            "description": ""
        },
        {
            "id": "MONDO:0008746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008746",
            "name": "albinism 2",
            "description": ""
        },
        {
            "id": "MONDO:0008746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008746",
            "name": "albinism, Brown oculocutaneous",
            "description": ""
        },
        {
            "id": "MONDO:0008746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008746",
            "name": "Albinoidism",
            "description": ""
        },
        {
            "id": "MONDO:0008746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008746",
            "name": "oculocutaneous albinism, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0008746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008746",
            "name": "oculocutaneous albinism tyrosinase positive",
            "description": ""
        },
        {
            "id": "MONDO:0008746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008746",
            "name": "OCA2",
            "description": ""
        },
        {
            "id": "MONDO:0008746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008746",
            "name": "albinism, oculocutaneous, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0008746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008746",
            "name": "tyrosinase-positive oculocutaneous albinism",
            "description": ""
        },
        {
            "id": "MONDO:0008746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008746",
            "name": "oculocutaneous albinism type II",
            "description": ""
        },
        {
            "id": "MONDO:0008746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008746",
            "name": "oculocutaneous albinism, tyrosinase-positive",
            "description": ""
        },
        {
            "id": "MONDO:0008746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008746",
            "name": "albinism, oculocutaneous, type II; OCA2",
            "description": ""
        },
        {
            "id": "MONDO:0008746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008746",
            "name": "albinism, oculocutaneous, type II",
            "description": ""
        },
        {
            "id": "MIM:203200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/203200",
            "name": "Albinism, oculocutaneous, 2",
            "description": "Albinism, oculocutaneous, 2"
        }
    ]
}