{
    "disease_id": "DOID:0070098", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011683", 
            "name": "oculocutaneous albinism type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011683", 
            "name": "albinism, oculocutaneous, type IV; OCA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011683", 
            "name": "SLC45A2 oculocutaneous albinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011683", 
            "name": "albinism, oculocutaneous, type IV"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011683", 
            "name": "oculocutaneous albinism caused by mutation in SLC45A2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011683", 
            "name": "oculocutaneous albinism, type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011683", 
            "name": "OCA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011683", 
            "name": "albinism, oculocutaneous, type 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070098", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070098", 
            "name": "OCA4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070098", 
        "description": "An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of SLC45A2 on chromosome 5p13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070098", 
        "name": "oculocutaneous albinism type IV"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070098#disease-associations", 
            "id": "0070098", 
            "database": "Alliance of Genome Resources"
        }
    ]
}