Serine biosynthesis pathway deficiency, infantile/juvenile form 1284855000
SNOMED CT code
SNOMED code | 1284855000 |
---|---|
name | Serine biosynthesis pathway deficiency, infantile/juvenile form |
status | active |
date introduced | 2023-05-31 |
fully specified name(s) | Serine biosynthesis pathway deficiency, infantile/juvenile form (disorder) |
synonyms | Serine biosynthesis pathway deficiency, infantile/juvenile form |
attributes - group1 | |
Occurrence | Congenital 255399007 |
attributes - group2 | |
Finding site | Nervous system structure 25087005 |
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 Serine biosynthesis pathway deficiency, infantile/juvenile form 1284855000 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 Serine biosynthesis pathway deficiency, infantile/juvenile form 1284855000 |
ancestors | sorted most to least specific
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cpt crosswalks |
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