PEX1 deficiency 1187532002
SNOMED CT code
SNOMED code | 1187532002 |
---|---|
name | PEX1 deficiency |
status | active |
date introduced | 2022-01-31 |
fully specified name(s) | Peroxisome biogenesis disorder due to PEX1 mutation (disorder) |
synonyms |
|
attributes - group1 | |
Occurrence | Congenital 255399007 |
parents | Peroxisome biogenesis disorder 742876007 |
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 Peroxisome biogenesis disorder 742876007 PEX1 deficiency 1187532002 |
ancestors | sorted most to least specific
|
cpt crosswalks |
Thank you for choosing Find-A-Code, please Sign In to remove ads.