{
    "disease_id": "DOID:0110008", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "Pingelapese blindness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "ACHM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "achromatopsia 3; ACHM3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "rod monochromacy 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "CNGB3 achromatopsia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "RMCH1 (formerly)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "total colorblindness with myopia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "Rod monochromatism 1 (formerly)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "rod monochromatism 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "ACHM3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "rod monochromatism 1, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "achromatopsia caused by mutation in CNGB3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "achromatopsia type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "RMCH1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "Rod monochromacy 1 (formerly)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "achromatopsia with myopia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "ACHM1 (formerly)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "ACHM1, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009875", 
            "name": "rod monochromacy 1, formerly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110008", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110008", 
            "name": "ACHM1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110008", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110008", 
            "name": "ACHM3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110008", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110008", 
            "name": "Pingelapese blindness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110008", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110008", 
            "name": "RMCH1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110008", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110008", 
            "name": "rod monochromacy 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110008", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110008", 
            "name": "rod monochromatism 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110008", 
        "description": "An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGB3 gene on chromosome 8q2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110008", 
        "name": "achromatopsia 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110008#disease-associations", 
            "id": "0110008", 
            "database": "Alliance of Genome Resources"
        }
    ]
}