ORPHA:231641

Rare non surgically correctable form of primary aldosteronism

Type: Category
Group: Group of disorders
Inheritance: Autosomal dominant, Not applicable
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.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Rare non surgically correctable form of primary aldosteronism
fr	Hyperaldostéronisme primitif rare non traitable chirurgicalement
de	Seltene chirurgisch nicht korrigierbar Formen des primären Hyperaldosteronismus
es	Hiperaldosteronismo primario raro no corregible por cirugía
it	Iperaldosteronismo primitivo raro non corregibile chirugicamente
nl	Zeldzame niet-chirurgisch corrigeerbare vorm van primair aldosteronisme
pt	Hiperaldosteronismo primário raro não corrigível cirurgicamente
pl	Rzadka forma pierwotnego aldosteronizmu niemożliwa do korekcji chirurgicznej
cs	Vzácná nechirurgicky korigovatelná forma primárního aldosteronismu
uk	Рідкісна форма первинного альдостеронізму, що не піддається хірургічній корекції
zh	罕见非手术可纠正型原发性醛固酮症
tr	Primer aldosteronizmin nadir cerrahi olarak düzeltilemeyen formu

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	16508	E		validated
UMLS	C5680926	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:97978Rare endocrine disease

Parents in the classifications (1):

ORPHA:181415Rare primary hyperaldosteronism
rare endocrine diseases

Children (2):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/231641
This record as JSON: /data/d/231641.json