Vohwinkel syndrome

Summary

Vohwinkel syndrome is a genodermatosis^[1].

Key Facts

• Vohwinkel syndrome's instance of is recorded as genodermatosis^[2].
• Vohwinkel syndrome's instance of is recorded as rare disease^[3].
• Vohwinkel syndrome's instance of is recorded as class of disease^[4].
• Vohwinkel syndrome's subclass of is recorded as palmoplantar keratosis^[5].
• Vohwinkel syndrome's subclass of is recorded as syndromic genetic deafness^[6].
• Vohwinkel syndrome's subclass of is recorded as autosomal dominant diffuse mutilating palmoplantar keratoderma^[7].
• Vohwinkel syndrome's subclass of is recorded as autosomal dominant disease^[8].
• Vohwinkel syndrome's subclass of is recorded as syndrome^[9].
• Vohwinkel syndrome's subclass of is recorded as head and neck disease^[10].
• Vohwinkel syndrome's subclass of is recorded as developmental defect during embryogenesis^[11].
• Vohwinkel syndrome's MeSH descriptor ID is recorded as C536457^[12].
• Vohwinkel syndrome's OMIM ID is recorded as 124500^[13].
• Vohwinkel syndrome's ICD-10 ID is recorded as Q82.8^[14].
• Vohwinkel syndrome's DiseasesDB is recorded as 32216^[15].
• Vohwinkel syndrome's KEGG ID is recorded as H00714^[16].
• Vohwinkel syndrome's eMedicine ID is recorded as 1108458^[17].
• Vohwinkel syndrome's Disease Ontology ID is recorded as DOID:0111339^[18].
• Vohwinkel syndrome's mode of inheritance is recorded as autosomal dominant^[19].
• Vohwinkel syndrome's Orphanet ID is recorded as 494^[20].
• Vohwinkel syndrome's ICD-9-CM is recorded as 757.39^[21].
• Vohwinkel syndrome's health specialty is recorded as medical genetics^[22].
• Vohwinkel syndrome's genetic association is recorded as GJB2^[23].
• Vohwinkel syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_494^[24].
• Vohwinkel syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111339^[25].
• Vohwinkel syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111339^[26].