raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2245

OBSOLETE: Hypopituitarism-postaxial polydactyly syndrome

inactive · referred to ORPHA:420584Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Hypopituitarism-postaxial polydactyly syndrome
frOBSOLETE : Syndrome d'hypopituitarisme-polydactylie postaxiale
deOBSOLET: Hypopituitarismus - postaxiale PolydaktylieOBSOLET: Culler-Jones-Syndrom
esOBSOLETO: Síndrome de hipopituitarismo-polidactilia postaxialOBSOLETO: Síndrome de Culler-Jones
itOBSOLETO: Ipopituitarismo - polidattilia postassialeOBSOLETO: Sindrome di Culler-Jones
nlOBSOLEET: Hypopituïtarisme - postaxiale polydactylie-syndroomOBSOLEET: Syndroom van Culler-Jones
ptOBSOLETO: Síndrome de hipopituitarismo-polidactilia pós-axialOBSOLETO: Síndrome Culler-Jones
plNIEAKTUALNE: Niedoczynnosc przysadki - polidaktylia zaosiowaNIEAKTUALNE: Zespół Cullera i Jonesa
csNEAKTUÁLNÍ: Syndrom zahrnující hypopituitarismus a postaxiální polydaktyliiNEAKTUÁLNÍ: Cullerův-Jonesův syndrom · NEAKTUÁLNÍ: Culler-Jonesův syndrom
ukЗАСТАРІЛО: Синдром гіпопітуїтаризму- постаксіальної полідактилії
zh弃用:垂体机能减退-轴后性多指(趾)综合征
trEski adı: Hipopituitarizm-postaksiyal polidaktili sendromu
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

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