{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007850", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007850", 
            "name": "Kid syndrome, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007850", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007850", 
            "name": "keratitis-ichthyosis-deafness syndrome, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007850", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007850", 
            "name": "autosomal dominant KID syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060871", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060871", 
            "name": "autosomal dominant KID syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/148210", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:148210", 
            "name": "Keratitis-ichthyosis-deafness syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060871", 
        "description": "A syndrome characterized by congenital deafness, keratopachydermia and constrictions of fingers and toes that has material_basis_in heterozygous mutation in the GJB2 gene on chromosome 13q.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060871", 
        "name": "autosomal dominant keratitis-ichthyosis-deafness syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/148210", 
            "id": "148210", 
            "database": "MIM"
        }
    ]
}