autosomal recessive palmoplantar keratoderma and congenital alopecia (Q55781720)
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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
Language | Label | Description | Also known as |
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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 |
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