{
    "disease_id": "DOID:0070100", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014070", 
            "name": "oculocutaneous albinism type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014070", 
            "name": "OCA7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014070", 
            "name": "oculocutaneous albinism caused by mutation in LRMDA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014070", 
            "name": "albinism, oculocutaneous, type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014070", 
            "name": "albinism, oculocutaneous, type VII; OCA7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014070", 
            "name": "albinism, oculocutaneous, type VII"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014070", 
            "name": "LRMDA oculocutaneous albinism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070100", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070100", 
            "name": "OCA7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070100", 
        "description": "An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of C10orf11 on chromosome 10q22.2-q22.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070100", 
        "name": "oculocutaneous albinism type VII"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070100#disease-associations", 
            "id": "0070100", 
            "database": "Alliance of Genome Resources"
        }
    ]
}