raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:178025

Non-acquired combined pituitary hormone deficiencies without extrapituitary malformations

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
enNon-acquired combined pituitary hormone deficiencies without extrapituitary malformations
frInsuffisance hypophysaire multiple non acquise sans malformations extra-hypophysaires associées
deHypophysenhormon-Mangel, nicht erworbener, kombinierter, ohne assoziierte extrahypophysäre Fehlbildung
esDeficiencia combinada de hormonas hipofisarias no adquirida sin malformaciones extrahipofisarias
itDeficit non acquisiti degli ormoni ipofisari, non associati a difetti extraipofisari
nlNiet-verworven gecombineerde hypofysehormoondeficiënties zonder extra-hypofysaire malformaties
ptDeficiências de hormona hipofisária não adquiridas combinadas sem malformações extra-hipofisáriasDeficiências de hormona pituitária não adquiridas combinadas sem malformações extra-pituitárias
plNienabyty złożony Niedobór hormonów przysadki bez malformacji pozaprzysadkowych
csNezískané kombinované deficity hormonů hypofýzy bez dalších malformací hypofýzy
ukНенабутий комбінований дефіцит гормонів гіпофіза без екстрагіпофізарних вад розвитку
zh非获得性联合垂体激素缺乏不伴垂体外畸形
trEkstrapituiter malformasyonlar olmayan edinilmemiş kombine hipofiz hormonu eksiklikleri
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO15789Evalidated
UMLSC5680506Evalidated

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