Hereditary growth hormone deficiency 1186807002
SNOMED CT code
| SNOMED code | 1186807002 |
|---|---|
| name | Hereditary growth hormone deficiency |
| status | active |
| date introduced | 2021-11-30 |
| fully specified name(s) | Hereditary growth hormone deficiency (disorder) |
| synonyms | Hereditary growth hormone deficiency |
| attributes - group1 | |
| Finding site | Structure of distal part of pituitary 52618001 |
| parents | |
| children |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Hereditary growth hormone deficiency 1186807002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Hereditary growth hormone deficiency 1186807002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Disorder of pituitary gland 399244003 Disorder of anterior pituitary 51742006 Growth hormone deficiency 397827003 Hereditary growth hormone deficiency 1186807002 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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