{
    "disease_id": "DOID:0110867",
    "recommended_name": {
        "id": "DOID:0110867",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110867",
        "name": "congenital stationary night blindness 1C",
        "description": "A congenital stationary night blindness characterized by autosomal recessive that has_material_basis_in homozygous or compound heterozygous mutation in the TRPM1 gene on chromosome 15q13-q14."
    },
    "synonyms": [
        {
            "id": "DOID:0110867",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110867",
            "name": "CSNB1C",
            "description": ""
        },
        {
            "id": "DOID:0110867",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110867",
            "name": "congenital stationary night blindness 1C autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0013183",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013183",
            "name": "congenital stationary night blindness 1C",
            "description": "Any congenital stationary night blindness in which the cause of the disease is a mutation in the TRPM1 gene."
        },
        {
            "id": "MONDO:0013183",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013183",
            "name": "congenital stationary night blindness type 1C",
            "description": ""
        },
        {
            "id": "MONDO:0013183",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013183",
            "name": "night blindness, congenital stationary, type 1C; CSNB1C",
            "description": ""
        },
        {
            "id": "MONDO:0013183",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013183",
            "name": "night blindness, congenital stationary, type 1C",
            "description": ""
        },
        {
            "id": "MONDO:0013183",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013183",
            "name": "congenital stationary night blindness 1C autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0013183",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013183",
            "name": "TRPM1 congenital stationary night blindness",
            "description": ""
        },
        {
            "id": "MONDO:0013183",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013183",
            "name": "CSNB1C",
            "description": ""
        },
        {
            "id": "MONDO:0013183",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013183",
            "name": "congenital stationary night blindness caused by mutation in TRPM1",
            "description": ""
        },
        {
            "id": "MONDO:0013183",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013183",
            "name": "CSNB, complete, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:613216",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613216",
            "name": "Night blindness, congenital stationary, 1C",
            "description": "Night blindness, congenital stationary, 1C"
        }
    ]
}