Megacystis, microcolon, hypoperistalsis syndrome 253781004
SNOMED CT code
| SNOMED code | 253781004 |
|---|---|
| name | Megacystis, microcolon, hypoperistalsis syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Megacystis, microcolon, hypoperistalsis syndrome (disorder) |
| synonyms |
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| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Dilatation 25322007 |
| Finding site | Urinary bladder structure 89837001 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Colon structure 71854001 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Congenital smallness 41086002 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Bowel finding 249562008 Finding of large intestine 118436003 Disorder of large intestine 119523007 Congenital anomaly of large intestine 1492007 Megacystis, microcolon, hypoperistalsis syndrome 253781004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Megacystis, microcolon, hypoperistalsis syndrome 253781004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital functional disorders of the colon 253778009 Megacystis, microcolon, hypoperistalsis syndrome 253781004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Megacystis, microcolon, hypoperistalsis syndrome 253781004 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Megacystis, microcolon, hypoperistalsis syndrome 253781004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Hereditary disorder of the urinary system 363338001 Megacystis, microcolon, hypoperistalsis syndrome 253781004 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Bowel finding 249562008 Finding of large intestine 118436003 Disorder of large intestine 119523007 Motility disorder of large intestine 737198009 Megacystis, microcolon, hypoperistalsis syndrome 253781004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Megacystis, microcolon, hypoperistalsis syndrome 253781004 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Pelvic organ finding 700006000 Urinary bladder finding 249585009 Bladder distention 54768000 Congenital dilatation of urinary bladder 93052002 Megacystis, microcolon, hypoperistalsis syndrome 253781004 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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