A group of autosomal dominant, autosomal recessive, X-linked inherited or acquired disorders characterized by the thickening of the palms and soles due to hyperkeratosis. [ NCIT:C34748 ]
Synonyms: keratosis palmaris et plantaris palmoplantar keratoderma
This is just here as a test because I lose it
Term information
database
cross reference
- EFO:1000745 (MONDO:equivalentTo)
- DOID:3390 (MONDO:equivalentTo)
- ICD9:757.39 (MONDO:relatedTo)
- NCIT:C34748 (MONDO:equivalentTo)
- SCTID:706885006 (MONDO:equivalentTo)
exactMatch
http://purl.obolibrary.org/obo/NCIT_C34748
http://identifiers.org/snomedct/706885006
http://purl.obolibrary.org/obo/DOID_3390