raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2950

Triphalangeal thumb-polysyndactyly syndrome

inactive · moved to ORPHA:988Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome

Synonyms: TPT-PS syndrome

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enTriphalangeal thumb-polysyndactyly syndromeTPT-PS syndrome
frSyndrome de pouce triphalangé-polysyndactylieSyndrome TPT-PS
deTriphalangeale Daumen-Polysyndaktylie-SyndromTPT-PS
esSíndrome de pulgar trifalángico-polisindactiliaSíndrome TPT-PS
itSindrome da pollice trifalangeo-polisindattiliaSindrome TPT-PS
nlTrifalangeale duim - polysyndactylie-syndroomTPT-PS-syndroom
ptSíndrome de polegar trifalângico-polissindactiliaSíndrome TPT-PS
plZespół trójpaliczkowy kciuk - polisyndaktyliaZespół TPT-PS
csSyndrom zahrnující tříčlánkový palec na ruce a polysyndaktyliiTPT-PS syndrom
ukСиндром трифалангової полісиндактилії великого пальцяСиндром TPT-PS
zh三指节拇指-多指(趾)并指(趾)综合征TPT-PS综合征
trTrifalanjiyal başparmak-polisindaktili sendromTPT-PS sendromu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MeSHC536563Evalidated

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

3

Classification

Not placed in any Orphanet classification in this release.

No children.

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