{
    "disease_id": "DOID:0111339",
    "recommended_name": {
        "id": "DOID:0111339",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111339",
        "name": "Vohwinkel syndrome",
        "description": "A syndrome characterized by severe, honeycomb-patterned palmoplantar keratosis, constrictions on the fingers and toes leading to autoamputation and mild to moderate congenital sensorineural hearing loss that has_material_basis_in heterozygous mutation in GJB2 on chromosome 13q12.11."
    },
    "synonyms": [
        {
            "id": "DOID:0111339",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111339",
            "name": "KHM",
            "description": ""
        },
        {
            "id": "DOID:0111339",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111339",
            "name": "Mutilating keratoderma plus deafness",
            "description": ""
        },
        {
            "id": "DOID:0111339",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111339",
            "name": "PPK mutilans and deafness",
            "description": ""
        },
        {
            "id": "DOID:0111339",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111339",
            "name": "VOWNKL",
            "description": ""
        },
        {
            "id": "DOID:0111339",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111339",
            "name": "keratoderma hereditarium mutilans",
            "description": ""
        },
        {
            "id": "DOID:0111339",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111339",
            "name": "mutilating keratoderma of Vohwinkel",
            "description": ""
        },
        {
            "id": "DOID:0111339",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111339",
            "name": "congenital deafness with keratopachydermia and constrictions fo fingers and toes",
            "description": ""
        },
        {
            "id": "MONDO:0007422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007422",
            "name": "keratoderma hereditarium mutilans",
            "description": ""
        },
        {
            "id": "MONDO:0007422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007422",
            "name": "mutilating keratoderma of Vohwinkel",
            "description": ""
        },
        {
            "id": "MONDO:0007422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007422",
            "name": "PPK mutilans and deafness",
            "description": ""
        },
        {
            "id": "MONDO:0007422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007422",
            "name": "keratoderma hereditarium mutilans",
            "description": ""
        },
        {
            "id": "MONDO:0007422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007422",
            "name": "mutilating keratoderma plus deafness",
            "description": ""
        },
        {
            "id": "MONDO:0007422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007422",
            "name": "Vohwinkel syndrome; VOWNKL",
            "description": ""
        },
        {
            "id": "MONDO:0007422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007422",
            "name": "KHM",
            "description": ""
        },
        {
            "id": "MONDO:0007422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007422",
            "name": "Vohwinkel syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007422",
            "name": "VOWNKL",
            "description": ""
        },
        {
            "id": "MONDO:0007422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007422",
            "name": "mutilating keratoderma",
            "description": ""
        },
        {
            "id": "MONDO:0007422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007422",
            "name": "deafness, congenital, with KERATOPACHYDERMIA and constrictions of fingers and toes",
            "description": ""
        },
        {
            "id": "MIM:124500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/124500",
            "name": "Vohwinkel syndrome",
            "description": "Vohwinkel syndrome"
        }
    ]
}