PEX13 deficiency 1187527003
SNOMED CT code
SNOMED code | 1187527003 |
---|---|
name | PEX13 deficiency |
status | active |
date introduced | 2022-01-31 |
fully specified name(s) | Peroxisome biogenesis disorder due to PEX13 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 PEX13 deficiency 1187527003 |
ancestors | sorted most to least specific
|
cpt crosswalks |
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