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69478001: Pancreatic colipase deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
115426011 Pancreatic colipase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
809427011 Pancreatic colipase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pancreatic colipase deficiency Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Pancreatic colipase deficiency Is a Malabsorption syndrome false Inferred relationship Existential restriction modifier
Pancreatic colipase deficiency Is a Enzymopathy true Inferred relationship Existential restriction modifier
Pancreatic colipase deficiency Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier
Pancreatic colipase deficiency Is a Congenital anomaly of digestive system false Inferred relationship Existential restriction modifier
Pancreatic colipase deficiency Is a Disorder of pancreas false Inferred relationship Existential restriction modifier
Pancreatic colipase deficiency Is a Disorder of lipid storage and metabolism false Inferred relationship Existential restriction modifier
Pancreatic colipase deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Pancreatic colipase deficiency Finding site Structure of small intestine false Inferred relationship Existential restriction modifier 1
Pancreatic colipase deficiency Finding site Pancreatic structure false Inferred relationship Existential restriction modifier 1
Pancreatic colipase deficiency Is a Pancreatic malabsorption true Inferred relationship Existential restriction modifier
Pancreatic colipase deficiency Is a Congenital anomaly of pancreas false Inferred relationship Existential restriction modifier
Pancreatic colipase deficiency Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier
Pancreatic colipase deficiency Finding site Structure of digestive system false Inferred relationship Existential restriction modifier 1
Pancreatic colipase deficiency Finding site Digestive organ structure false Inferred relationship Existential restriction modifier 1
Pancreatic colipase deficiency Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Pancreatic colipase deficiency Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Pancreatic colipase deficiency Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier
Pancreatic colipase deficiency Is a Congenital anomaly of digestive tract false Inferred relationship Existential restriction modifier
Pancreatic colipase deficiency Is a Congenital anomaly of small intestine false Inferred relationship Existential restriction modifier
Pancreatic colipase deficiency Finding site Structure of small intestine false Inferred relationship Existential restriction modifier 1
Pancreatic colipase deficiency Finding site Pancreatic structure false Inferred relationship Existential restriction modifier 1
Pancreatic colipase deficiency Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Pancreatic colipase deficiency Finding site Pancreatic structure true Inferred relationship Existential restriction modifier 2
Pancreatic colipase deficiency Finding site Structure of small intestine true Inferred relationship Existential restriction modifier 1
Pancreatic colipase deficiency Is a Hereditary disorder of endocrine system true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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