Multiple carboxylase deficiency - neonatal onset 360367001
SNOMED CT code
SNOMED code | 360367001 |
---|---|
name | Multiple carboxylase deficiency - neonatal onset |
status | removed |
date introduced | 2002-01-31 |
date removed | 2003-07-31 |
fully specified name(s) | Multiple carboxylase deficiency - neonatal onset (disorder) |
synonyms | Multiple carboxylase deficiency - neonatal onset |
parents | Biotin-(propionyl-CoA-carboxylase) ligase deficiency 15307001 removed: 2020-07-31 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Biotin-(propionyl-CoA-carboxylase) ligase deficiency 15307001 removed: 2020-07-31 Multiple carboxylase deficiency - neonatal onset 360367001 removed: 2003-07-31 |
ancestors | sorted most to least specific |
cpt crosswalks |
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