Hereditary butyrylcholinesterase deficiency 1296959007
SNOMED CT code
SNOMED code | 1296959007 |
---|---|
name | Hereditary butyrylcholinesterase deficiency |
status | active |
date introduced | 2023-12-01 |
fully specified name(s) | Hereditary butyrylcholinesterase deficiency (disorder) |
synonyms |
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attributes - group2 | |
Due to | Deficiency of butyrylcholinesterase 360619001 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
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 recessive hereditary disorder 85995004 Hereditary butyrylcholinesterase deficiency 1296959007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Hereditary butyrylcholinesterase deficiency 1296959007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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