Sarcosine dehydrogenase deficiency 64852002
SNOMED CT code
| SNOMED code | 64852002 |
|---|---|
| name | Sarcosine dehydrogenase deficiency |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Sarcosine dehydrogenase deficiency (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 Sarcosine dehydrogenase deficiency 64852002 SNOMED CT Concept 138875005 Clinical 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 glycine metabolism 83076007 Sarcosine dehydrogenase deficiency 64852002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Sarcosine dehydrogenase deficiency 64852002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Sarcosine dehydrogenase deficiency 64852002 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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