{
    "disease_id": "DOID:0110009", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014677", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014677", 
            "name": "achromatopsia caused by mutation in ATF6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014677", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014677", 
            "name": "ACHM7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014677", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014677", 
            "name": "ATF6 achromatopsia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014677", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014677", 
            "name": "achromatopsia 7; ACHM7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014677", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014677", 
            "name": "achromatopsia type 7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110009", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110009", 
            "name": "ACHM7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110009", 
        "description": "An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the ATF6 gene on chromosome 1q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110009", 
        "name": "achromatopsia 7"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616517", 
            "id": "616517", 
            "database": "MIM"
        }
    ]
}