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autosomal recessive palmoplantar keratoderma and congenital alopecia

Disease Summary
Associated Targets (0)

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Mondo Description 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.
Mondo Term and Equivalent IDs
MONDO:0008923:  autosomal recessive palmoplantar keratoderma and congenital alopecia
DOID:0111245: 
GARD:0001139: 
MESH:C535336: 
Orphanet:1366: 
UMLS:C1859316: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found