Moderate steroid 21-hydroxylase deficiency 60045007
SNOMED CT code
SNOMED code | 60045007 |
---|---|
name | Moderate steroid 21-hydroxylase deficiency |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Moderate steroid 21-hydroxylase deficiency (disorder) |
synonyms | Moderate steroid 21-hydroxylase deficiency |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Adrenal cortex structure 68594002 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of steroid metabolism 28710006 Deficiency of steroid 21-monooxygenase 124221007 Moderate steroid 21-hydroxylase deficiency 60045007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Moderate steroid 21-hydroxylase deficiency 60045007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Moderate steroid 21-hydroxylase deficiency 60045007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Moderate steroid 21-hydroxylase deficiency 60045007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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