hereditary palmoplantar keratoderma
Go to external page http://purl.obolibrary.org/obo/MONDO_0019272
An instance of palmoplantar keratosis that is caused by an inherited modification of the individual's genome. [ MONDO:patterns/hereditary ]
Synonyms: hereditary keratosis palmoplantaris hereditary palmoplantar keratosis hereditary PPK hereditary palmoplantar hyperkeratosis
Term information
- ICD9:757.39 (MONDO:relatedTo)
- Orphanet:79357 (MONDO:equivalentTo)
- MEDGEN:590657 (MONDO:equivalentTo)
- SCTID:239066003 (MONDO:equivalentTo)
- GARD:18988 (MONDO:GARD)
- icd11.foundation:1941547119 (https://orcid.org/0000-0001-5208-3432)
- UMLS:C0406757 (MONDO:equivalentTo)
gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders
http://www.orpha.net/ORDO/Orphanet_79357
http://identifiers.org/medgen/590657
http://identifiers.org/snomedct/239066003
http://linkedlifedata.com/resource/umls/id/C0406757