OMOP Concept 435508
Adrenal cortical hypofunction
StandardConditionSNOMED386584007Disorder
Maps from
24
Descendants
49
Valid from
31 Jan 2003
Valid to
31 Dec 2099
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Source codes that map to this concept
24 source codes normalize to Adrenal cortical hypofunction via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Adrenal cortical hypofunction across source vocabularies.
- Adrenal cortical hypofunction (disorder)
- Adrenal insufficiency
- Adrenocortical hypofunction
- Corticoadrenal insufficiency
- hipofunción de corteza adrenal
- hipofunción de corteza adrenal (trastorno)
- Hypoadrenocorticism
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Disorder of adrenal cortex
- 1Hypoadrenalism
- 2Disorder of adrenal gland
- 3Abdominal organ finding
- 3Disorder of endocrine system
- 3Disorder of retroperitoneum
- 4Disorder of abdomen
- 4Disorder of body system
- 4Finding of abdomen
- 4Viscus structure finding
- 5Clinical finding
- 5Disease
- 5Disorder of abdominopelvic segment of trunk
- 5Finding of abdominopelvic segment of trunk
- 6Disorder of trunk
- 6Finding of trunk structure
Narrower concepts
(49)Included automatically when you query with descendants.
- 1Acute adrenal insufficiency
- 1Addison's disease
- 1Adrenal cortical hypofunction due to interruption of corticosteroid therapy
- 1Adrenal insufficiency due to adrenal metastasis
- 1Adrenocortical hypofunction following procedure
- 1Adrenoleukodystrophy
- 1Adrenomyodystrophy
- 1Aldosterone deficiency
- 1Atypical hypoadrenocorticism
- 1Congenital hypoplasia of adrenal gland
- 1Congenital primary adrenocortical hypofunction
- 1Drug-induced adrenocortical insufficiency
- 1Hereditary adrenal unresponsiveness to corticotropin
- 1Hypocortisolism secondary to another disorder
- 1Iatrogenic adrenal insufficiency
- 1Primary adrenocortical insufficiency
- 1Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency
- 1Pseudohypoaldosteronism, type 1
- 1Severe adrenal insufficiency
- 1Testicular hypofunction due to defect in adrenocortical hormone synthesis
- 1Waterhouse-Friderichsen syndrome
- 2Addison's disease due to autoimmunity
- 2Addison's disease with adrenoleucodystrophy
- 2Adolescent X-linked adrenoleukodystrophy
- 2Adrenocorticotropic hormone resistance syndrome
- 2Adrenomyeloneuropathy
- 2Childhood cerebral X-linked adrenoleukodystrophy
- 2Congenital adrenal hypoplasia, X-linked
- 2Corticosterone 18-monooxygenase deficiency
- 2Familial adrenal hypoplasia with absent pituitary luteinizing hormone
- 2Familial adrenocortical hypoplasia
- 2Familial hypoaldosteronism
- 2Familial steroid-resistant nephrotic syndrome with adrenal insufficiency
- 2Hyperreninemic hypoaldosteronism
- 2Hyporeninemic hypoaldosteronism
- 2Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency
- 2MIRAGE syndrome
- 2Neonatal adrenoleukodystrophy
- 2Polyglandular autoimmune syndrome, type 1
- 2Post-adrenalectomy adrenal insufficiency
- 2Pseudohypoaldosteronism, type 1, dominant form
- 2Pseudohypoaldosteronism, type 1, recessive form
- 2Tuberculous Addison's disease
- 2Xp21 deletion syndrome
- 3Familial glucocorticoid deficiency
- 3Familial hyperreninemic hypoaldosteronism type 1A
- 3Familial hyperreninemic hypoaldosteronism type 1B
- 3Familial hyperreninemic hypoaldosteronism type 2
- 3Glucocorticoid deficiency with achalasia
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