FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

37992001: Pancreatic insufficiency (disorder)


Status: current, Not 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
63364014 Pancreatic insufficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
769953018 Pancreatic insufficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1859921000195112 insufficienza pancreatica it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
288751000172118 insuffisance pancréatique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


6 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Exocrine pancreatic insufficiency Is a True Pancreatic insufficiency Inferred relationship Some
Shwachman syndrome Is a True Pancreatic insufficiency Inferred relationship Some
Other pancreatic secretion disorder Is a False Pancreatic insufficiency Inferred relationship Some
Pancreatic insufficiency due to cystic fibrosis of pancreas (disorder) Is a True Pancreatic insufficiency Inferred relationship Some
Secondary pancreatic insufficiency (disorder) Is a True Pancreatic insufficiency Inferred relationship Some
A rare multiple congenital anomalies/dysmorphic syndrome with intellectual disability characterized by global developmental delay, postnatal microcephaly, intellectual disability, ataxia, sensorineural hearing loss, and exocrine pancreatic insufficiency. More variable manifestations include hypotonia, growth retardation, peripheral demyelinating neuropathy, dysmorphic facial features, and additional endocrine abnormalities. Brain imaging may show progressive cerebellar atrophy in some patients. Is a True Pancreatic insufficiency Inferred relationship Some

This concept is not in any reference sets

Back to Start