Laron-type isolated somatotropin defect 38196001
SNOMED CT code
| SNOMED code | 38196001 |
|---|---|
| name | Laron-type isolated somatotropin defect |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Laron-type isolated somatotropin defect (disorder) |
| synonyms |
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| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group2 | |
| Interprets | Height / growth measure 271603002 |
| parents | |
| children | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 Laron-type isolated somatotropin defect 38196001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Laron-type isolated somatotropin defect 38196001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Laron-type isolated somatotropin defect 38196001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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