Familial hypercholanemia 723360007
SNOMED CT code
SNOMED code | 723360007 |
---|---|
name | Familial hypercholanemia |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Familial hypercholanemia (disorder) |
synonyms |
|
attributes - group2 | |
Occurrence | Congenital 255399007 |
attributes - group1 | |
Finding site | Liver structure 10200004 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Familial disease 111941005 Familial hypercholanemia 723360007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic and genetic disorder affecting the liver 235903001 Synthetic defect of bile acids 235915002 Familial hypercholanemia 723360007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Familial hypercholanemia 723360007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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