{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011749", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011749", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011749", 
            "name": "albinism, Yellow mutant type"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011749", 
            "name": "Oca1-Ts"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011749", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011749", 
            "name": "albinism, oculocutaneous, type IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011749", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011749", 
            "name": "platinum oculocutaneous albinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011749", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011749", 
            "name": "oculocutaneous albinism, Amish type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011749", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011749", 
            "name": "albinism, oculocutaneous, type 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011749", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011749", 
            "name": "albinism, oculocutaneous, type I, temperature-sensitive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011749", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011749", 
            "name": "Yellow albinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011749", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011749", 
            "name": "OCA1B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070095", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070095", 
            "name": "Albinism, Yellow Mutant Type"
        }, 
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            "description": "", 
            "resource": "Disease Ontology", 
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        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:606952", 
            "name": "Albinism, oculocutaneous, 1B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070095", 
        "description": "An oculocutaneous albinism that has_material_basis_in an autosomal recessive hypomorphic mutation of TYR on chromosome 11q14.3 with retention of some residual protein activity.", 
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        "id": "DOID:0070095", 
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    }, 
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            "database": "MIM"
        }
    ]
}