OMOP Concept 196369
Adrenogenital disorder
StandardConditionSNOMED267395000Disorder
Maps from
36
Descendants
38
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
36 source codes normalize to Adrenogenital disorder via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Adrenogenital disorder across source vocabularies.
- Adrenogenital disorder (disorder)
- Adrenogenital syndrome
- Androgenital syndrome
- síndrome adrenogenital
- trastorno adrenogenital
- trastorno adrenogenital (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Disorder of adrenal gland
- 2Abdominal organ finding
- 2Disorder of endocrine system
- 2Disorder of retroperitoneum
- 3Disorder of abdomen
- 3Disorder of body system
- 3Finding of abdomen
- 3Viscus structure finding
- 4Clinical finding
- 4Disease
- 4Disorder of abdominopelvic segment of trunk
- 4Finding of abdominopelvic segment of trunk
- 5Disorder of trunk
- 5Finding of trunk structure
Narrower concepts
(38)Included automatically when you query with descendants.
- 1Acquired adrenogenital syndrome
- 1Congenital adrenal hyperplasia
- 1Drug-induced adrenogenital disorder
- 1Feminization-adrenogenital syndrome
- 1Feminizing syndrome of adrenal origin
- 1Generalized glucocorticoid resistance syndrome
- 1Hyperandrogenism due to cortisone reductase deficiency
- 1Iatrogenic adrenogenital disorder
- 1Idiopathic adrenogenital disorder
- 1MIRAGE syndrome
- 1Testicular lesion of adrenogenital syndrome
- 1Virilizing syndrome of adrenal origin
- 23 beta-Hydroxysteroid dehydrogenase deficiency
- 2Achard-Thiers syndrome
- 2Acquired benign adrenal androgenic overactivity
- 2CAH - desmolase deficiency
- 2Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- 2Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency
- 2Congenital lipoid adrenal hyperplasia due to STAR deficiency
- 2Corticosterone 18-monooxygenase deficiency
- 2Deficiency of steroid 11-beta-monooxygenase
- 2Deficiency of steroid 17-alpha-monooxygenase
- 2Hereditary glucocorticoid resistance
- 2Late onset congenital adrenal hyperplasia
- 2Pseudohermaphrodite, male with adrenocortical disorder
- 2Salt-losing congenital adrenal hyperplasia
- 2Salt-losing congenital adrenal hyperplasia with virilism
- 2Steroid 21-monooxygenase deficiency, simple virilizing type
- 2Testosterone 17-beta-dehydrogenase deficiency
- 2Virilization-adrenogenital syndrome
- 2Virilizing adrenal tumor
- 317 alpha-Hydroxyprogesterone aldolase deficiency
- 3Cholesterol monooxygenase (side-chain cleaving) deficiency
- 3Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency classic form
- 3Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency non classic form
- 3Female adrenal virilization
- 3Pseudohermaphrodite, female with adrenocortical disorder
- 3Steroid 21-monooxygenase deficiency, salt wasting type
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