Phosphoserine aminotransferase deficiency 718603002
SNOMED CT code
SNOMED code | 718603002 |
---|---|
name | Phosphoserine aminotransferase deficiency |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | Deficiency of phosphoserine aminotransferase (disorder) |
synonyms |
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parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Phosphoserine aminotransferase deficiency 718603002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 Specific enzyme deficiency 129456006 Deficiency of aminotransferase 124394008 Phosphoserine aminotransferase deficiency 718603002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of organic acid metabolism 116021002 Disorder of amino acid metabolism 44779003 Disorder of amino acid and organic acid metabolism 237911005 Disorder of serine metabolism 303097007 Phosphoserine aminotransferase deficiency 718603002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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