raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:95618

Pituitary hormone deficiency secondary to storage 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 storage disease
frInsuffisance hypophysaire secondaire à une maladie de surcharge
deHypophysenhormon-Mangel, sekundärer, bei Speicherkrankheit
esDeficiencia de la hormona hipofisaria, secundaria a una enfermedad por almacenamiento
itDeficit degli ormoni pituitari secondaria a malattia da accumulo
nlDeficiëntie van hypofysehormoon secundair aan stapelingsziekte
ptDeficiência da hormona pituitária secundária a doença de armazenamento
plNiedobór hormonów przysadki wtórny do choroby spichrzeniowej
csSekundární deficit hormonů hypofýzy z důvodu střádavého onemocnění
ukДефіцит гормонів гіпофіза внаслідок хвороби накопичення
zh积贮病继发垂体激素缺乏症
trDepo hastalığına bağlı hipofiz hormonu eksikliği
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5681565Evalidated

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