raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:95701

OBSOLETE: Congenital adrenal hypoplasia of maternal cause

inactive · referred to ORPHA:101963Acquired chronic primary adrenal insufficiency

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Acquired chronic primary adrenal insufficiency

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Congenital adrenal hypoplasia of maternal cause
frOBSOLETE : Hypoplasie surrénalienne congénitale de cause maternelle
deOBSOLET: Nierenhypoplasie, kongenitale, maternalen Ursprungs
esOBSOLETO: Hipoplasia adrenal congénita de origen materno
itOBSOLETO: Ipoplasia surrenalica congenita con origine materna
nlOBSOLEET: Congenitale adrenale hypoplasie van maternale oorzaakOBSOLEET: Congenitale bijnierhypoplasie van maternale oorzaak
ptOBSOLETO: Hipoplasia supra-renal congénita de causa materna
plNIEAKTUALNE: Wrodzona hipoplazja nadnerczy z przyczyn matczynych
csNEAKTUÁLNÍ: Vrozená adrenální hypoplázie z maternálních příčin
ukЗАСТАРІЛО: Вроджена гіпоплазія надниркових залоз по материнській лінії
zh弃用:母源性先天性肾上腺发育不良
trEski adı: Maternal kaynaklı doğumsal adrenal hipoplazi
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