Vohwinkel syndrome
human disease
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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 is a type of palmoplantar keratosis[5].
- Vohwinkel syndrome is a type of syndromic genetic deafness[6].
- Vohwinkel syndrome is a type of autosomal dominant diffuse mutilating palmoplantar keratoderma[7].
- Vohwinkel syndrome is a type of autosomal dominant disease[8].
- Vohwinkel syndrome is a type of syndrome[9].
- Vohwinkel syndrome is a type of head and neck disease[10].
- Vohwinkel syndrome is a type of developmental defect during embryogenesis[11].
- Vohwinkel syndrome's mode of inheritance is recorded as autosomal dominant[12].
- Vohwinkel syndrome's ICD-9-CM is recorded as 757.39[13].
- Vohwinkel syndrome's health specialty is recorded as medical genetics[14].
- Vohwinkel syndrome's genetic association is recorded as GJB2[15].
- Vohwinkel syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_494[16].
- Vohwinkel syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111339[17].
- Vohwinkel syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111339[18].