ORPHA:641613

Endogenous Cushing syndrome

Synonyms: Endogenous CS

Type: Category
Group: Group of disorders
Status: active

A rare group of endocrine disorders caused by prolonged and high exposure levels to glucocorticoids of endogenous (adrenal cortex production) origin. Typical clinical features are truncal and facial obesity, hypercatabolic syndrome (thinned skin, purple striae, ecchymosis, bruising with no obvious trauma, proximal muscle weakness with amyotrophy, osteoporosis) and, in children, weight gain with decreasing growth velocity.

Names in Orphadata languages

10 of 12 languages

Lang	Name	Synonyms
en	Endogenous Cushing syndrome	Endogenous CS
fr	Syndrome de Cushing endogène
de	Cushing-Syndrom, endogenes	Endogenes CS
es	Síndrome de Cushing endógeno	SC endógeno
it	Sindrome di Cushing endogena	SC endogena
nl	Endogeen syndroom van Cushing	Endogeen CS
pt	Síndrome Cushing endógena	CS endógena
pl	Rzadki endogenny zespół Cushinga	Endogenny zespół Cushinga
cs	Endogenní Cushingův syndrom	= en
uk	Ендогенний синдром Кушинга	Ендогенний CS

Definition in:

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	0957431	E		validated
UMLS	C5419158	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):

Codes that Orphanet moved or referred to this one:

ORPHA:553OBSOLETE: Cushing syndrome referred to · inactive

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/641613
This record as JSON: /data/d/641613.json