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66972006: Protein-losing enteropathy (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
111243018 Protein-losing enteropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
806644016 Protein-losing enteropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1232865010 PLE - Protein-losing enteropathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4609131000241117 entéropathie avec perte de protéines fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Protein-losing enteropathy Is a Malabsorption syndrome true Inferred relationship Some
Protein-losing enteropathy Finding site Structure of small intestine (body structure) true Inferred relationship Some 1
Protein-losing enteropathy Is a Disorder of small intestine true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital chronic diarrhoea with protein-losing enteropathy is a rare, genetic, intestinal disease characterised by early-onset, chronic, non-infectious, non-bloody, watery diarrhoea associated with protein-losing enteropathy which results in hypoalbuminaemia, hypogammaglobulinaemia and elevated stool alpha-1-antitrypsin. Patients typically present severe, intractable diarrhoea, failure to thrive, recurrent infections and oedema. Is a True Protein-losing enteropathy Inferred relationship Some
Protein losing enteropathy due to and following cardiac procedure (disorder) Is a True Protein-losing enteropathy Inferred relationship Some
A rare genetic disease characterized by CD55 deficiency with complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy with abdominal pain, diarrhea, vomiting, primary intestinal lymphangiectasia, hypoproteinemic edema, and malabsorption, leading to anemia and growth delay. Bowel inflammation and recurrent infections associated with hypogammaglobulinemia may also be observed. Is a True Protein-losing enteropathy Inferred relationship Some

This concept is not in any reference sets

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