{
    "disease_id": "DOID:0050632",
    "recommended_name": {
        "id": "DOID:0050632",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050632",
        "name": "oculocutaneous albinism",
        "description": "A syndrome characterized by abnormal pigmentation of the skin, hair and eyes."
    },
    "synonyms": [
        {
            "id": "MONDO:0008745",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008745",
            "name": "oculocutaneous albinism type 1A",
            "description": "Oculocutaneous albinism type 1A (OCA1A) is the most severe form of OCA, where no melanin is produced, and is characterized by white hair and skin, blue, fully translucent irises, nystagmus and misrouting of the optic nerves."
        },
        {
            "id": "MONDO:0008745",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008745",
            "name": "OCA1A",
            "description": ""
        },
        {
            "id": "MONDO:0008745",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008745",
            "name": "TYR oculocutaneous albinism",
            "description": ""
        },
        {
            "id": "MONDO:0008745",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008745",
            "name": "Tyr oculocutaneous albinism",
            "description": ""
        },
        {
            "id": "MONDO:0008745",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008745",
            "name": "oculocutaneous albinism caused by mutation in TYR",
            "description": ""
        },
        {
            "id": "MONDO:0008745",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008745",
            "name": "oculocutaneous albinism caused by mutation in Tyr",
            "description": ""
        },
        {
            "id": "MONDO:0008745",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008745",
            "name": "oculocutaneous albinism, tyrosinase-negative",
            "description": ""
        },
        {
            "id": "MONDO:0008745",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008745",
            "name": "tyrosinase-negative oculocutaneous albinism",
            "description": ""
        },
        {
            "id": "MONDO:0008745",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008745",
            "name": "albinism, oculocutaneous, type IA",
            "description": ""
        },
        {
            "id": "MIM:203100",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/203100",
            "name": "Albinism, oculocutaneous, 1A",
            "description": "Albinism, oculocutaneous, 1A"
        }
    ],
    "children": [
        {
            "id": "DOID:0070094",
            "label": "oculocutaneous albinism type IA",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070095",
            "label": "oculocutaneous albinism type IB",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070096",
            "label": "oculocutaneous albinism type II",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070097",
            "label": "oculocutaneous albinism type III",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070098",
            "label": "oculocutaneous albinism type IV",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070100",
            "label": "oculocutaneous albinism type VII",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0080614",
            "label": "oculocutaneous albinism type VI",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0070094",
        "DOID:0070097",
        "DOID:0070098",
        "DOID:0050632",
        "DOID:0070095",
        "DOID:0070100",
        "DOID:0080614",
        "DOID:0070096"
    ],
    "unlinked_id_list": []
}