Renal hepatic pancreatic dysplasia 763891005
SNOMED CT code
| SNOMED code | 763891005 |
|---|---|
| name | Renal hepatic pancreatic dysplasia |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Renal hepatic pancreatic dysplasia (disorder) |
| synonyms |
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| attributes - group3 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of parenchyma of liver 127879008 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Pancreatic structure 15776009 |
| Associated morphology | Fibrosis 112674009 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Polycystic change 3679006 |
| Finding site | Kidney structure 64033007 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Digestive system finding 386617003 Finding of pancreas 300357002 Disorder of pancreas 3855007 Congenital malformation of pancreas 235977001 Renal hepatic pancreatic dysplasia 763891005 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Finding of pancreas 300357002 Disorder of pancreas 3855007 Fibrosis of pancreas 25942009 Renal hepatic pancreatic dysplasia 763891005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Renal hepatic pancreatic dysplasia 763891005 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Renal hepatic pancreatic dysplasia 763891005 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 Renal hepatic pancreatic dysplasia 763891005 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Renal hepatic pancreatic dysplasia 763891005 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Congenital anomaly of the kidney 44513007 Renal hepatic pancreatic dysplasia 763891005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Renal hepatic pancreatic dysplasia 763891005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital renal cyst 369071000119105 Multiple congenital cysts of kidney 82525005 Renal hepatic pancreatic dysplasia 763891005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Renal hepatic pancreatic dysplasia 763891005 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Liver finding 249565005 Disease of liver 235856003 Congenital anomaly of liver 89166001 Renal hepatic pancreatic dysplasia 763891005 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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