{
    "disease_id": "DOID:11661",
    "recommended_name": {
        "id": "DOID:11661",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:11661",
        "name": "blue color blindness",
        "description": "A color blindness that is characterised by a selective deficiency of blue vision, has_material_basis_in autosomal dominant inheritance of a mutation in the OPN1SW gene and is associated with a deficiency or absence of blue-sensitive cone photoreceptor function."
    },
    "synonyms": [
        {
            "id": "DOID:11661",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11661",
            "name": "Tritan defect",
            "description": ""
        },
        {
            "id": "DOID:11661",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11661",
            "name": "Tritanopia",
            "description": ""
        },
        {
            "id": "MONDO:0008610",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008610",
            "name": "blue color blindness",
            "description": "Tritanopia is an extremely rare form of colour blindness characterised by a selective deficiency of blue vision."
        },
        {
            "id": "MONDO:0008610",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008610",
            "name": "blue colorblindness",
            "description": ""
        },
        {
            "id": "MONDO:0008610",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008610",
            "name": "congenital tritanopia",
            "description": ""
        },
        {
            "id": "MONDO:0008610",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008610",
            "name": "colorblindness, tritanopic",
            "description": ""
        },
        {
            "id": "MONDO:0008610",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008610",
            "name": "tritanopia",
            "description": ""
        },
        {
            "id": "MONDO:0008610",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008610",
            "name": "tritan defect",
            "description": ""
        },
        {
            "id": "MONDO:0008610",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008610",
            "name": "tritan colour blindness",
            "description": ""
        },
        {
            "id": "MONDO:0008610",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008610",
            "name": "colorblindness, tritan",
            "description": ""
        },
        {
            "id": "MONDO:0008610",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008610",
            "name": "blue colour blindness",
            "description": ""
        },
        {
            "id": "MIM:190900",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/190900",
            "name": "Tritan color blindness",
            "description": "Tritan color blindness"
        }
    ]
}