ORPHA:181415

Rare primary hyperaldosteronism

Synonyms: Rare primary aldosteronism

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.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Rare primary hyperaldosteronism	Rare primary aldosteronism
fr	Hyperaldostéronisme primitif rare	Aldostéronisme primitif rare
de	Hyperaldosteronismus, primärer, seltener	Aldosteronismus, primärer, seltener
es	Hiperaldosteronismo primario raro	Aldosteronismo primario raro
it	Iperaldosteronismo primitivo raro	Aldosteronismo primitivo raro
nl	Zeldzaam primair hyperaldosteronisme	Zeldzaam primair aldosteronisme
pt	Hiperaldosteronismo raro
pl	Rzadki pierwotny hiperaldosteronizm	Rzadki pierwotny aldosteronizm
cs	Vzácný primární hyperaldosteronismus	Vzácný primární aldosteronismus
uk	Рідкісний первинний гіперальдостеронізм	Рідкісний первинний альдостеронізм
zh	罕见原发性醛固酮增多症	罕见原发性醛固酮增多症
tr	Nadir primer hiperaldosteronizm	Nadir primer aldosteronizm

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	15899	E		validated
UMLS	C5679597	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:101954Rare adrenal disease
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/181415
This record as JSON: /data/d/181415.json