3-phosphoglycerate dehydrogenase deficiency juvenile form 733636005
SNOMED CT code
| SNOMED code | 733636005 |
|---|---|
| name | 3-phosphoglycerate dehydrogenase deficiency juvenile form |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | 3-phosphoglycerate dehydrogenase deficiency juvenile form (disorder) |
| synonyms | 3-phosphoglycerate dehydrogenase deficiency juvenile form |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Central nervous system structure 21483005 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Inherited metabolic disorder of nervous system 128190004 3-phosphoglycerate dehydrogenase deficiency juvenile form 733636005 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 3-phosphoglycerate dehydrogenase deficiency juvenile form 733636005 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 serine metabolism 303097007 3-Phosphoglycerate dehydrogenase deficiency 303098002 3-phosphoglycerate dehydrogenase deficiency juvenile form 733636005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 3-phosphoglycerate dehydrogenase deficiency juvenile form 733636005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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