{
    "disease_id": "DOID:0111339", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007422", 
            "name": "keratoderma hereditarium mutilans"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007422", 
            "name": "mutilating keratoderma of Vohwinkel"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007422", 
            "name": "PPK mutilans and deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007422", 
            "name": "mutilating keratoderma plus deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007422", 
            "name": "Vohwinkel syndrome; VOWNKL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007422", 
            "name": "KHM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007422", 
            "name": "VOWNKL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007422", 
            "name": "mutilating keratoderma"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007422", 
            "name": "deafness, congenital, with KERATOPACHYDERMIA and constrictions of fingers and toes"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111339", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111339", 
            "name": "KHM"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111339", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111339", 
            "name": "Mutilating keratoderma plus deafness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111339", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111339", 
            "name": "PPK mutilans and deafness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111339", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111339", 
            "name": "VOWNKL"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111339", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111339", 
            "name": "keratoderma hereditarium mutilans"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111339", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111339", 
            "name": "mutilating keratoderma of Vohwinkel"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111339", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111339", 
            "name": "congenital deafness with keratopachydermia and constrictions fo fingers and toes"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111339", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111339", 
        "name": "Vohwinkel syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111339#disease-associations", 
            "id": "0111339", 
            "database": "Alliance of Genome Resources"
        }
    ]
}