{
    "disease_id": "DOID:0060871",
    "recommended_name": {
        "id": "DOID:0060871",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060871",
        "name": "autosomal dominant keratitis-ichthyosis-deafness syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060871",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060871",
            "name": "autosomal dominant KID syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007850",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007850",
            "name": "autosomal dominant keratitis-ichthyosis-deafness syndrome",
            "description": "Autosomal dominant form of KID syndrome."
        },
        {
            "id": "MONDO:0007850",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007850",
            "name": "Kid syndrome, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0007850",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007850",
            "name": "keratitis-ichthyosis-deafness syndrome, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0007850",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007850",
            "name": "KID syndrome, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0007850",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007850",
            "name": "autosomal dominant KID syndrome",
            "description": ""
        },
        {
            "id": "MIM:148210",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/148210",
            "name": "Keratitis-ichthyosis-deafness syndrome, autosomal dominant",
            "description": "Keratitis-ichthyosis-deafness syndrome, autosomal dominant"
        }
    ]
}