raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:95617

Pituitary hormone deficiency secondary to a granulomatous disease

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
enPituitary hormone deficiency secondary to a granulomatous disease
frInsuffisance hypophysaire d'origine granulomateuse
deHypophysenhormon-Mangel, sekundärer, bei Granulomatose
esDeficiencia de la hormona hipofisaria secundaria a enfermedad granulomatosa
itDeficit degli ormoni pituitari secondaria a malattia granulomatosa
nlHypofysehormoondeficiëntie secundair aan een granulomateuze ziekte
ptDeficiência de hormona pituitária secundária a doença granulomatosa
plNiedobór hormonów przysadki wtórny do choroby ziarniniakowej
csSekundární deficit hormonů hypofýzy z důvodu granulomatózního onemocnění
ukДефіцит гормонів гіпофіза внаслідок гранулематозного захворювання
zh肉芽肿性疾病继发垂体激素缺乏症
trGranülomatöz bir hastalığa bağlı sekonder hipofiz hormonu eksikliği
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5681566Evalidated

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 (1):

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