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25942009: Fibrosis of pancreas (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
43471011 Fibrosis of pancreas en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
43472016 Cirrhosis of pancreas en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
756317012 Fibrosis of pancreas (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4473841000241112 fibrose du pancréas fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fibrosis of pancreas Is a Disorder of pancreas true Inferred relationship Some
Fibrosis of pancreas Associated morphology Fibrosis false Inferred relationship Some 1
Fibrosis of pancreas Finding site Pancreatic structure (body structure) false Inferred relationship Some 1
Fibrosis of pancreas Finding site Structure of digestive system (body structure) false Inferred relationship Some
Fibrosis of pancreas Associated morphology Fibrosis true Inferred relationship Some 1
Fibrosis of pancreas Finding site Pancreatic structure (body structure) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Chronic fibrosing pancreatitis Is a True Fibrosis of pancreas Inferred relationship Some
Renal-hepatic-pancreatic dysplasia is a rare, genetic, developmental defect during embryogenesis syndrome characterized by 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-dependent diabetes. Is a True Fibrosis of pancreas Inferred relationship Some

This concept is not in any reference sets

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