(Q55781720)
(Redirected from Q66084942)
English
autosomal recessive palmoplantar keratoderma and congenital alopecia
ectodermal dysplasia characterized by autosomal recessive inheritance of alopecia, progressive palmoplantar hyperkeratosis resulting in sclerodactyly and usually associated with cataracts and pseudoainhum formation
- PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2
- palmoplantar keratoderma and congenital alopecia, Wallis type
- PPKCA Wallis type
- Cataract, alopecia, sclerodactyly syndrome
- Autosomal recessive palmoplantar hyperkeratosis and congenital alopecia
- PPKCA2
- palmoplantar keratoderma and congenital alopecia 2
- autosomal recessive palmoplantar hyperkeratosis and congenital alopecia
- Cataract-Alopecia-Sclerodactyly Syndrome
- Cataract, alopecia, sclerodactyly
- Palmoplantar Keratoderma and Congenital Alopecia type 2
- Ppkca, Wallis Type
- CASS
- PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2; PPKCA2
- cataract-alopecia-sclerodactyly syndrome
- PPK-CA, Wallis type
- Palmoplantar keratoderma and congenital alopecia, Wallis type
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