{
    "disease_id": "DOID:0050679", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "blue cone monochromacy; BCM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "X-chromosome-linked achromatopsia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "S cone monochromatism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "X-linked achromatopsia incomplete"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "incomplete achromatopsia X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "colorblindness, blue-Mono-cone-monochromatic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "blue cone monochromatism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "cone dystrophy 5, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "achromatopsia incomplete X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "S cone monochromacy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "X-linked incomplete achromatopsia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "BCM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "CBBM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "color blindness, blue monocone monochromatic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "atypical X-linked achromatopsia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010563", 
            "name": "color blindness blue mono cone monochromatic type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050679", 
        "description": "An achromatopsia that is characterized by severely impaired color discrimination, low visual acuity, nystagmus, photophobia due to the absence of functional long wavelength-sensitive and medium wavelength-sensitive cones in the retina and has_material_basis_in recessive X-linked inheritance.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050679", 
        "name": "blue cone monochromacy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/303700", 
            "id": "303700", 
            "database": "MIM"
        }
    ]
}