{
    "disease_id": "DOID:11661", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008610", 
            "name": "blue colorblindness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008610", 
            "name": "congenital tritanopia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008610", 
            "name": "colorblindness, tritanopic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008610", 
            "name": "tritanopia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008610", 
            "name": "tritan defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008610", 
            "name": "tritan colour blindness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008610", 
            "name": "colorblindness, tritan"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008610", 
            "name": "blue colour blindness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11661", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11661", 
            "name": "Tritan defect"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11661", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11661", 
            "name": "Tritanopia"
        }, 
        {
            "url": "https://www.omim.org/entry/190900", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:190900", 
            "name": "Tritan color blindness"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:11661", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:11661", 
        "name": "blue color blindness"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/190900", 
            "id": "190900", 
            "database": "MIM"
        }
    ]
}