{
    "disease_id": "DOID:0110007", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009003", 
            "name": "Rod monochromacy 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009003", 
            "name": "colorblindness, total"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009003", 
            "name": "achromatopsia 2; ACHM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009003", 
            "name": "ACHM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009003", 
            "name": "CNGA3 achromatopsia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009003", 
            "name": "Rod monochromatism 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009003", 
            "name": "achromatopsia type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009003", 
            "name": "achromatopsia caused by mutation in CNGA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009003", 
            "name": "RMCH2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110007", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110007", 
            "name": "ACHM2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110007", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110007", 
            "name": "RMCH2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110007", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110007", 
            "name": "rod monochromacy 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110007", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110007", 
            "name": "rod monochromatism 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110007", 
        "description": "An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110007", 
        "name": "achromatopsia 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110007#disease-associations", 
            "id": "0110007", 
            "database": "Alliance of Genome Resources"
        }
    ]
}