Term info
database cross reference
- SCTID:239066003 (MONDO:equivalentTo)
- Orphanet:79357 (MONDO:equivalentTo)
- ICD9:757.39 (MONDO:relatedTo)
Subsets
disease_grouping, ordo_group_of_disorders
definition
An instance of palmoplantar keratosis that is caused by an inherited modification of the individual's genome.
exactMatch
http://identifiers.org/snomedct/239066003, http://purl.obolibrary.org/obo/Orphanet_79357
has exact synonym
hereditary keratosis palmoplantaris, hereditary palmoplantar keratosis, hereditary PPK, hereditary palmoplantar hyperkeratosis
id
MONDO:0019272