Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form 840509001
SNOMED CT code
| SNOMED code | 840509001 |
|---|---|
| name | Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form |
| status | active |
| date introduced | 2020-07-31 |
| fully specified name(s) | Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form (disorder) |
| synonyms | Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form |
| attributes - group1 | |
| Finding site | Adrenal cortex structure 68594002 |
| Associated morphology | Hyperplasia 76197007 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group2 | |
| Due to | Deficiency of steroid 21-monooxygenase 124221007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Disorder of adrenal gland 30171000 Disorder of adrenal cortex 129636003 Adrenocortical hyperplasia 237777008 Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form 840509001 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Disorder of adrenal gland 30171000 Congenital anomaly of adrenal gland 60637003 Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form 840509001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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