OMOP Concept 201399
Congenital anomaly of adrenal gland
StandardConditionSNOMED60637003Disorder
Maps from
15
Descendants
44
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
15 source codes normalize to Congenital anomaly of adrenal gland via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 144261 | Congenital anomaly of adrenal gland | Non-standard |
| CIM10 | Q89.1 | Congenital malformations of adrenal gland | Non-standard |
| ICD10 | Q89.1 | Congenital malformations of adrenal gland | Non-standard |
| ICD10CM | Q89.1 | Congenital malformations of adrenal gland | Non-standard |
| ICD10CN | Q89.1 | Congenital malformations of adrenal gland | Non-standard |
| ICD10CN | Q89.100 | Congenital malformations of adrenal gland | Non-standard |
| ICD10CN | Q89.101 | Ectopic adrenal (machine translation) | Non-standard |
| ICD10GM | Q89.1 | Congenital malformations of adrenal gland | Non-standard |
| ICD9CM | 759.1 | Anomalies of adrenal gland | Non-standard |
| KCD7 | Q89.1 | Congenital malformations of adrenal gland | Non-standard |
| Nebraska Lexicon | 60637003 | Congenital malformation of adrenal gland | Non-standard |
| Read | PK1..00 | Anomalies of adrenal gland | Non-standard |
| Read | PK1y.00 | Other specified anomalies of adrenal gland | Non-standard |
| Read | PK1yz00 | Other congenital anomaly of adrenal gland NOS | Non-standard |
| Read | PK1z.00 | Anomalies of adrenal gland NOS | Non-standard |
Synonyms
Alternative names recorded for Congenital anomaly of adrenal gland across source vocabularies.
- anomalía congénita de glándula adrenal
- anomalía congénita de glándula suprarrenal
- anomalía congénita de glándula suprarrenal (trastorno)
- Congenital anomaly of adrenal gland (disorder)
- Congenital malformation of adrenal gland
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(23)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of abdomen
- 1Congenital anomaly of endocrine gland
- 1Disorder of adrenal gland
- 2Abdominal organ finding
- 2Congenital anomaly of lower trunk
- 2Congenital malformation
- 2Disorder of abdomen
- 2Disorder of endocrine system
- 2Disorder of retroperitoneum
- 3Congenital abnormality of lower limb and pelvic girdle
- 3Congenital anomaly of trunk
- 3Congenital disease
- 3Developmental disorder
- 3Disorder of abdominopelvic segment of trunk
- 3Disorder of body system
- 3Finding of abdomen
- 3Viscus structure finding
- 4Clinical finding
- 4Disease
- 4Disorder of fetus and/or newborn
- 4Disorder of trunk
- 4Finding of abdominopelvic segment of trunk
- 5Finding of trunk structure
Narrower concepts
(44)Included automatically when you query with descendants.
- 1Accessory adrenal gland
- 1Congenital abnormal fusion of adrenal glands
- 1Congenital abnormal shape of adrenal gland
- 1Congenital absence of adrenal gland
- 1Congenital adrenal hyperplasia
- 1Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form
- 1Congenital cyst of adrenal gland
- 1Congenital hypertrophy of adrenal gland
- 1Congenital hypoplasia of adrenal gland
- 1Congenital malposition of adrenal gland
- 1Ectopic adrenal gland
- 1SERKAL syndrome
- 23 beta-Hydroxysteroid dehydrogenase deficiency
- 2Accessory adrenal cortex
- 2Aplasia of adrenal gland
- 2CAH - desmolase deficiency
- 2Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- 2Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency
- 2Congenital adrenal hypoplasia, X-linked
- 2Congenital lipoid adrenal hyperplasia due to STAR deficiency
- 2Corticosterone 18-monooxygenase deficiency
- 2Deficiency of steroid 11-beta-monooxygenase
- 2Deficiency of steroid 17-alpha-monooxygenase
- 2Ectopic adrenal cortex
- 2Extracapsular adrenal tissue
- 2Familial adrenal hypoplasia with absent pituitary luteinizing hormone
- 2Familial adrenocortical hypoplasia
- 2Familial steroid-resistant nephrotic syndrome with adrenal insufficiency
- 2Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency
- 2Late onset congenital adrenal hyperplasia
- 2MIRAGE syndrome
- 2Salt-losing congenital adrenal hyperplasia
- 2Salt-losing congenital adrenal hyperplasia with virilism
- 2Testosterone 17-beta-dehydrogenase deficiency
- 2Virilization-adrenogenital syndrome
- 2Xp21 deletion syndrome
- 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
- 3Steroid 21-monooxygenase deficiency, simple virilizing type
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