Methylcrotonyl-CoA carboxylase deficiency 13144005
SNOMED CT code
| SNOMED code | 13144005 |
|---|---|
| name | Methylcrotonyl-CoA carboxylase deficiency |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Methylcrotonyl-coenzyme A carboxylase deficiency (disorder) |
| synonyms |
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| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of organic acid metabolism 116021002 Disorder of amino acid metabolism 44779003 Disorder of amino acid and organic acid metabolism 237911005 Disorder of branched-chain amino acid metabolism 116020001 Methylcrotonyl-CoA carboxylase deficiency 13144005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of organic acid metabolism 116021002 Non-amino organic acidemia AND/OR aciduria 26513001 Methylcrotonyl-CoA carboxylase deficiency 13144005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 Methylcrotonyl-CoA carboxylase deficiency 13144005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Methylcrotonyl-CoA carboxylase deficiency 13144005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Methylcrotonyl-CoA carboxylase deficiency 13144005 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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