Term Name:	palmoplantar keratoderma and congenital alopecia 2
Synonyms:	autosomal recessive palmoplantar hyperkeratosis and congenital alopecia, autosomal recessive palmoplantar keratoderma and congenital alopecia, CASS, cataract-alopecia-sclerodactyly syndrome, palmoplantar keratoderma and congenital alopecia, Wallis type, PPK-CA, Wallis type, PPKCA Wallis type, PPKCA2
Definition:	An ectodermal dysplasia characterized by autosomal recessive inheritance of alopecia, progressive palmoplantar hyperkeratosis resulting in sclerodactyly and usually associated with cataracts and pseudoainhum formation.
Ontology:	Human Disease [DOID:0111245]   ( DOID:0111245 )