Hyperprolinemia type 2 717181004
SNOMED CT code
SNOMED code | 717181004 |
---|---|
name | Hyperprolinemia type 2 |
status | active |
date introduced | 2016-07-31 |
fully specified name(s) | Hyperprolinemia type 2 (disorder) |
synonyms |
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attributes - group1 | |
Due to | Deficiency of pyrroline-5-carboxylate reductase 124177001 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of acid-base balance 26436007 Acidemia 70731005 Aminoacidemia 46556004 Hyperprolinemia 59655002 Hyperprolinemia type 2 717181004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Hyperprolinemia type 2 717181004 |
ancestors | sorted most to least specific
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cpt crosswalks |
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