FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

717255008: Secondary intestinal lymphangiectasis (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3308844010 Secondary intestinal lymphangiectasia en Synonym Active Case insensitive SNOMED CT core
3308847015 Secondary intestinal lymphangiectasis en Synonym Active Case insensitive SNOMED CT core
3308848013 Secondary intestinal lymphangiectasis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
5168714010 An acquired form of intestinal lymphangiectasia manifesting as a protein-losing enteropathy due to another disorder such as Crohn disease, congestive heart failure, sarcoidosis, Turner syndrome and often in patients who have undergone a Fontan operation. It is characterized by malabsorption, diarrhea, edema due to hypoproteinemia, steatorrhea and serosal effusions. en Definition Active Case sensitive SNOMED CT core
5168715011 An acquired form of intestinal lymphangiectasia manifesting as a protein-losing enteropathy due to another disorder such as Crohn disease, congestive heart failure, sarcoidosis, Turner syndrome and often in patients who have undergone a Fontan operation. It is characterised by malabsorption, diarrhoea, oedema due to hypoproteinaemia, steatorrhoea and serosal effusions. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Secondary intestinal lymphangiectasis Is a Intestinal lymphangiectasis true Inferred relationship Some
Secondary intestinal lymphangiectasis Associated morphology Lymphangiectasis true Inferred relationship Some 1
Secondary intestinal lymphangiectasis Finding site Structure of lymphatic vessel of intestine true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start