GCGR-related hyperglucagonemia 1228875006
SNOMED CT code
SNOMED code | 1228875006 |
---|---|
name | GCGR-related hyperglucagonemia |
status | active |
date introduced | 2022-05-31 |
fully specified name(s) | Glucagon receptor-related hyperglucagonemia (disorder) |
synonyms |
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attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Structure of alpha cell of islet 61028007 |
Associated morphology | Hyperplasia 76197007 |
Pathological process | Pathological developmental process 308490002 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 GCGR-related hyperglucagonemia 1228875006 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 GCGR-related hyperglucagonemia 1228875006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 GCGR-related hyperglucagonemia 1228875006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 GCGR-related hyperglucagonemia 1228875006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital anomaly of endocrine gland 4184009 Islet cell hyperplasia 42681006 Hyperplasia of islet alpha cells with glucagon excess 87181002 GCGR-related hyperglucagonemia 1228875006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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