{
    "disease_id": "DOID:0111404", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009007", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009007", 
            "name": "cone rod dystrophy-amelogenesis imperfecta syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009007", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009007", 
            "name": "cone-Rod dystrophy and amelogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009007", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009007", 
            "name": "cone-rod dystrophy amelogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009007", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009007", 
            "name": "cone-rod dystrophy with amelogenesis imperfecta"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111404", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111404", 
            "name": "Cone rod dystrophy-amelogenesis imperfecta syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111404", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111404", 
            "name": "cone-rod dystrophy and amelogenesis imperfecta"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111404", 
        "description": "A syndrome characterized by amelogenesis imperfecta and cone-rod retinal dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in CNNM4 on chromosome 2q11.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111404", 
        "name": "Jalili syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111404#disease-associations", 
            "id": "0111404", 
            "database": "Alliance of Genome Resources"
        }
    ]
}