{
    "disease_id": "DOID:13911", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:13911", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13911", 
            "name": "ACHM"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13911", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13911", 
            "name": "Monochromatism"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:13911", 
        "description": "A color blindness that is characterized by a congenital cone color vision disorder, the inability to perceive color and to achieve satisfactory visual acuity at high light levels has_material_basis_in autosomal recessive inheritance.", 
        "resource": "Disease Ontology", 
        "id": "DOID:13911", 
        "name": "achromatopsia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/13911#disease-associations", 
            "id": "13911", 
            "database": "Alliance of Genome Resources"
        }
    ]
}