Phosphoenolpyruvate carboxykinase (GTP) deficiency 5335002
SNOMED CT code
SNOMED code | 5335002 |
---|---|
name | Phosphoenolpyruvate carboxykinase (GTP) deficiency |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Phosphoenolpyruvate carboxykinase deficiency (disorder) |
synonyms |
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attributes - group1 | |
Occurrence | Congenital 255399007 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 Specific enzyme deficiency 129456006 Phosphoenolpyruvate carboxykinase (GTP) deficiency 5335002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Disorder of pyruvate metabolism and mitochondrial respiratory chain 237981000 Inborn error of pyruvate metabolism 53210006 Phosphoenolpyruvate carboxykinase (GTP) deficiency 5335002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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