Hypermethioninemia due to deficiency of glycine N-methyltransferase 763720007
SNOMED CT code
| SNOMED code | 763720007 |
|---|---|
| name | Hypermethioninemia due to deficiency of glycine N-methyltransferase |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Hypermethioninemia due to deficiency of glycine N-methyltransferase (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 sulfur-bearing amino acid metabolism 28882002 Hypermethioninemia 43123004 Hypermethioninemia due to deficiency of glycine N-methyltransferase 763720007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hypermethioninemia due to deficiency of glycine N-methyltransferase 763720007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Hypermethioninemia due to deficiency of glycine N-methyltransferase 763720007 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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