palmoplantar keratoderma-deafness syndrome
medical condition
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palmoplantar keratoderma-deafness syndrome
Summary
palmoplantar keratoderma-deafness syndrome is a head and neck disease[1].
Key Facts
- palmoplantar keratoderma-deafness syndrome's instance of is recorded as head and neck disease[2].
- palmoplantar keratoderma-deafness syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- palmoplantar keratoderma-deafness syndrome's instance of is recorded as rare disease[4].
- palmoplantar keratoderma-deafness syndrome's instance of is recorded as class of disease[5].
- palmoplantar keratoderma-deafness syndrome is a type of syndromic genetic deafness[6].
- palmoplantar keratoderma-deafness syndrome is a type of autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature[7].
- palmoplantar keratoderma-deafness syndrome is a type of syndrome[8].
- palmoplantar keratoderma-deafness syndrome is a type of autosomal dominant disease[9].
- palmoplantar keratoderma-deafness syndrome's genetic association is recorded as GJB2[10].
- palmoplantar keratoderma-deafness syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2202[11].
- palmoplantar keratoderma-deafness syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111505[12].
- palmoplantar keratoderma-deafness syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111505[13].