Peroxisomal thiolase deficiency 238067002
SNOMED CT code
SNOMED code | 238067002 |
---|---|
name | Peroxisomal thiolase deficiency |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Peroxisomal thiolase deficiency (disorder) |
synonyms |
|
attributes - group1 | |
Occurrence | Congenital 255399007 |
parents | Loss of single peroxisomal function 238066006 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Disorder of peroxisomal function 238059005 Loss of single peroxisomal function 238066006 Peroxisomal thiolase deficiency 238067002 |
ancestors | sorted most to least specific
|
cpt crosswalks |
Thank you for choosing Find-A-Code, please Sign In to remove ads.