Familial hypertryptophanemia 721838005
SNOMED CT code
| SNOMED code | 721838005 |
|---|---|
| name | Familial hypertryptophanemia |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Familial hypertryptophanemia (disorder) |
| synonyms |
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| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Familial disease 111941005 Familial hypertryptophanemia 721838005 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 tryptophan metabolism 5181007 Tryptophanemia 237925006 Familial hypertryptophanemia 721838005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Familial hypertryptophanemia 721838005 |
| ancestors | sorted most to least specific
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| cpt crosswalks |
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