Severe primary trimethylaminuria 1237339005
SNOMED CT code
| SNOMED code | 1237339005 |
|---|---|
| name | Severe primary trimethylaminuria |
| status | active |
| date introduced | 2022-09-30 |
| fully specified name(s) | Severe primary trimethylaminuria (disorder) |
| synonyms | Severe primary trimethylaminuria |
| 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 Trimethylaminuria 237959005 Severe primary trimethylaminuria 1237339005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Severe primary trimethylaminuria 1237339005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Severe primary trimethylaminuria 1237339005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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