Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency 733447005
SNOMED CT code
SNOMED code | 733447005 |
---|---|
name | Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency (disorder) |
synonyms |
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attributes - group2 | |
Finding site | Structure of ileal lumen 40810008 |
Causative agent | Meconium stool 28112009 |
Occurrence | Early neonatal period 303114002 |
Associated morphology | Obstruction 26036001 |
attributes - group1 | |
Due to | Deficiency of guanylate cyclase 2C 733448000 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of fetus and/or newborn 414025005 Perinatal disorder 415073005 Fetal intrapartum and/or early neonatal disorder 1269435001 Meconium ileus 206523001 Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency 733447005 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Gastrointestinal tract finding 386618008 Disorder of gastrointestinal tract 119292006 Gastrointestinal complication 24813008 Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency 733447005 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency 733447005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency 733447005 |
ancestors | sorted most to least specific
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cpt crosswalks |
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