{
    "disease_id": "DOID:0070100",
    "recommended_name": {
        "id": "DOID:0070100",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070100",
        "name": "oculocutaneous albinism type VII",
        "description": "An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of C10orf11 on chromosome 10q22.2-q22.3."
    },
    "synonyms": [
        {
            "id": "DOID:0070100",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070100",
            "name": "OCA7",
            "description": ""
        },
        {
            "id": "MONDO:0014070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014070",
            "name": "oculocutaneous albinism type 7",
            "description": "Oculocutaneous albinism type 7 (OCA7), formerly called OCA5, is a form of oculocutaneous albinism (OCA; see this term) characterized by skin and hair hypopigmentation, nystagmus and iris transillumination."
        },
        {
            "id": "MONDO:0014070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014070",
            "name": "OCA7",
            "description": ""
        },
        {
            "id": "MONDO:0014070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014070",
            "name": "oculocutaneous albinism caused by mutation in LRMDA",
            "description": ""
        },
        {
            "id": "MONDO:0014070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014070",
            "name": "albinism, oculocutaneous, type 7",
            "description": ""
        },
        {
            "id": "MONDO:0014070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014070",
            "name": "albinism, oculocutaneous, type VII; OCA7",
            "description": ""
        },
        {
            "id": "MONDO:0014070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014070",
            "name": "albinism, oculocutaneous, type VII",
            "description": ""
        },
        {
            "id": "MONDO:0014070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014070",
            "name": "oculocutaneous albinism type VII",
            "description": ""
        },
        {
            "id": "MONDO:0014070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014070",
            "name": "LRMDA oculocutaneous albinism",
            "description": ""
        },
        {
            "id": "MIM:615179",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615179",
            "name": "Albinism, oculocutaneous, 7",
            "description": "Albinism, oculocutaneous, 7"
        }
    ]
}