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763891005: Renal hepatic pancreatic dysplasia (disorder)


Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3645159011 Renal hepatic pancreatic dysplasia (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3645160018 Renal hepatic pancreatic dysplasia en Synonym Active Case insensitive SNOMED CT core
3645161019 Ivemark II syndrome en Synonym Active Case sensitive SNOMED CT core
3645162014 Renohepaticopancreatic dysplasia en Synonym Active Case insensitive SNOMED CT core
3645163016 A rare genetic developmental defect during embryogenesis syndrome with the triad of pancreatic fibrosis (and cysts, with a reduction of parenchymal tissue), renal dysplasia (with peripheral cortical cysts, primitive collecting ducts, glomerular cysts and metaplastic cartilage) and hepatic dysgenesis (enlarged portal areas containing numerous elongated binary profiles with a tendency to perilobular fibrosis). Situs abnormalities, skeletal anomalies and anencephaly have also been associated. Patients that survive the neonatal period present renal insufficiency, chronic jaundice and insulin-dependant diabetes. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Renal hepatic pancreatic dysplasia Is a Congenital anomaly of pancreas true Inferred relationship Some
Renal hepatic pancreatic dysplasia Pathological process Pathological developmental process true Inferred relationship Some 3
Renal hepatic pancreatic dysplasia Pathological process Pathological developmental process true Inferred relationship Some 2
Renal hepatic pancreatic dysplasia Is a Congenital anomaly of the kidney true Inferred relationship Some
Renal hepatic pancreatic dysplasia Pathological process Pathological developmental process true Inferred relationship Some 1
Renal hepatic pancreatic dysplasia Associated morphology Morphologically abnormal structure true Inferred relationship Some 3
Renal hepatic pancreatic dysplasia Is a Hereditary disorder of endocrine system true Inferred relationship Some
Renal hepatic pancreatic dysplasia Is a Developmental hereditary disorder true Inferred relationship Some
Renal hepatic pancreatic dysplasia Is a Fibrosis of pancreas true Inferred relationship Some
Renal hepatic pancreatic dysplasia Is a Multiple system malformation syndrome true Inferred relationship Some
Renal hepatic pancreatic dysplasia Is a Polycystic kidney disease true Inferred relationship Some
Renal hepatic pancreatic dysplasia Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Renal hepatic pancreatic dysplasia Is a Congenital anomaly of liver true Inferred relationship Some
Renal hepatic pancreatic dysplasia Is a Digestive system hereditary disorder true Inferred relationship Some
Renal hepatic pancreatic dysplasia Is a Hereditary nephropathy true Inferred relationship Some
Renal hepatic pancreatic dysplasia Occurrence Congenital true Inferred relationship Some 3
Renal hepatic pancreatic dysplasia Associated morphology Developmental abnormality false Inferred relationship Some 3
Renal hepatic pancreatic dysplasia Finding site Structure of parenchyma of liver true Inferred relationship Some 3
Renal hepatic pancreatic dysplasia Occurrence Congenital true Inferred relationship Some 2
Renal hepatic pancreatic dysplasia Occurrence Congenital true Inferred relationship Some 1
Renal hepatic pancreatic dysplasia Associated morphology Polycystic change true Inferred relationship Some 1
Renal hepatic pancreatic dysplasia Finding site Kidney structure true Inferred relationship Some 1
Renal hepatic pancreatic dysplasia Finding site Pancreatic structure true Inferred relationship Some 2
Renal hepatic pancreatic dysplasia Associated morphology Fibrosis true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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