autosomal recessive disease autosomal recessive palmoplantar keratoderma and congenital alopecia https://rarediseases.info.nih.gov/diseases/1139/autosomal-recessive-palmoplantar-keratoderma-and-congenital-alopecia https://www.malacards.org/card/palmoplantar_keratoderma_and_congenital_alopecia_2 OMIM:212360 palmoplantar keratoderma and congenital alopecia type 2 PPK-CA, Wallis type Orphanet:1366 MEDGEN:347851 PPKCA2 palmoplantar keratoderma and congenital alopecia 2 cataract, alopecia, sclerodactyly syndrome DOID:0111245 GARD:0001139 cataract-alopecia-sclerodactyly syndrome Autosomal recessive palmoplantar hyperkeratosis and congenital alopecia (PPK-CA) is a rare genetic skin disorder characterized by congenital alopecia and palmoplantar hyperkeratosis. It is usually associated with cataracts, progressive sclerodactyly and pseudo-ainhum. cataract, alopecia, sclerodactyly cass autosomal recessive palmoplantar hyperkeratosis and congenital alopecia icd11.foundation:1733151457 MESH:C535336 Ppkca, Wallis type palmoplantar keratoderma and congenital alopecia, Wallis type MONDO:0008923 UMLS:C1859316 diffuse palmoplantar keratoderma ectodermal dysplasia syndrome