Hawkinsinuria 414380008
SNOMED CT code
| SNOMED code | 414380008 |
|---|---|
| name | Hawkinsinuria |
| status | active |
| date introduced | 2005-01-31 |
| fully specified name(s) | Hawkinsinuria (disorder) |
| synonyms | Hawkinsinuria |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Hawkinsinuria 414380008 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 sulfur-bearing amino acid metabolism 28882002 Hawkinsinuria 414380008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 4-Hydroxyphenylpyruvate dioxygenase deficiency 413356003 Hawkinsinuria 414380008 |
| ancestors | sorted most to least specific
|
| cpt crosswalks |
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com