Molybdenum cofactor deficiency complementation group C 1003387003
SNOMED CT code
SNOMED code | 1003387003 |
---|---|
name | Molybdenum cofactor deficiency complementation group C |
status | active |
date introduced | 2021-01-31 |
fully specified name(s) | Molybdenum cofactor deficiency complementation group C (disorder) |
synonyms | Molybdenum cofactor deficiency complementation group C |
attributes - group1 | |
Finding site | Kidney structure 64033007 |
parents | Combined molybdoflavoprotein enzyme deficiency 29692004 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Hereditary metabolic disease 1821000146108 Hereditary xanthinuria 54627004 Combined molybdoflavoprotein enzyme deficiency 29692004 Molybdenum cofactor deficiency complementation group C 1003387003 |
ancestors | sorted most to least specific
|
cpt crosswalks |
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