{
    "disease_id": "DOID:0070096", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008746", 
            "name": "oculocutaneous albinism type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008746", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008746", 
            "name": "albinism 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008746", 
            "name": "albinism, Brown oculocutaneous"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008746", 
            "name": "Albinoidism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008746", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008746", 
            "name": "oculocutaneous albinism tyrosinase positive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008746", 
            "name": "OCA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008746", 
            "name": "albinism, oculocutaneous, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008746", 
            "name": "tyrosinase-positive oculocutaneous albinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008746", 
            "name": "oculocutaneous albinism, tyrosinase-positive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008746", 
            "name": "albinism, oculocutaneous, type II; OCA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008746", 
            "name": "albinism, oculocutaneous, type II"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070096", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070096", 
            "name": "OCA2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070096", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070096", 
            "name": "Oculocutaneous Albinism, Tyrosinase-Positive"
        }, 
        {
            "url": "https://www.omim.org/entry/203200", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:203200", 
            "name": "Albinism, oculocutaneous, 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070096", 
        "description": "An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of OCA2 on chromosome 15q12-q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070096", 
        "name": "oculocutaneous albinism type II"
    }, 
    "evidence": [
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            "url": "https://www.omim.org/entry/203200", 
            "id": "203200", 
            "database": "MIM"
        }
    ]
}