raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:307967

Punctate palmoplantar keratoderma

Synonyms: Punctate PPK · Punctate keratosis palmoplantaris · Punctate palmoplantar hyperkeratosis

Type
Category
Group
Group of disorders
Status
active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enPunctate palmoplantar keratodermaPunctate PPK · Punctate keratosis palmoplantaris · Punctate palmoplantar hyperkeratosis
frKératodermie palmoplantaire ponctuéeHyperkératose palmoplantaire ponctuée · KPP ponctuée · PPK ponctuée
dePalmoplantarkeratose, punktiertePPK, punktierte · Palmoplantare Hyperkeratose, punktierte
esQueratodermia palmoplantar punctataHiperqueratosis palmoplantar punctata · PPK punctata · Queratosis palmoplantar punctata
itCheratoderma palmoplantare puntatoIpercheratosi palmoplantare puntata · Keratosis palmoplantaris puntata · PPK puntato
nlPuntvormige palmoplantaire keratodermiePuntvormige PPK · Puntvormige hyperkeratose van handpalm of voetzool · Puntvormige keratodermie van handpalm of voetzool · Puntvormige palmoplantaire hyperkeratose · Keratosis palmoplantaris punctata
ptQueratodermia palmoplantar punctiformeHiperqueratose palmoplantar punctiforme · PPK punctiforme · Queratose palmoplantar punctiforme
plRogowiec dłoniowo-podeszwowy punktowyHiperkertoza dłoniowo-podeszwowa punktowa · Punktowy PPK · Rogowacenie dłoniowo-podeszwowe punktowe
csKeratosis palmoplantaris punctataPPK puncata · Keratoderma palmoplantaris punctata · Hyperkeratosis palmoplantaris punctata
ukТОчкова долонно-підошовна кератодерміяПунктирний кератоз долонь · Пунктирний долонно-підошовний гіперкератоз · Punctate PPK
zh点状掌跖角化病点状掌跖角化病
trNoktalı palmoplantar keratodermaPunktata PPK · Punktata palmoplanter keratoz · Punktata palmoplantar hiperkeratoz
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0017675Evalidated
MONDO17675Evalidated
UMLSC1274216Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (2):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card