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1173999006: Interleukin 21 related infantile inflammatory bowel disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4639190012 Interleukin 21 related infantile inflammatory bowel disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4639191011 IL21-related infantile inflammatory bowel disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4639192016 Interleukin 21 related infantile inflammatory bowel disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4639193014 A rare autosomal recessive primary immunodeficiency characterised by infancy onset of severe inflammatory bowel disease with life-threatening diarrhoea and failure to thrive, oral aphthous ulcers, and recurrent severe upper and lower respiratory tract infections with finger clubbing. Laboratory examination reveals increased IgE and decreased IgG levels, as well as reduced numbers of circulating CD19+ B-cells including IgM+ naive and class-switched IgG memory B-cells, with a concomitant increase in transitional B-cells, while T-cell numbers and function are normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4639194015 A rare autosomal recessive primary immunodeficiency characterized by infancy onset of severe inflammatory bowel disease with life-threatening diarrhea and failure to thrive, oral aphthous ulcers, and recurrent severe upper and lower respiratory tract infections with finger clubbing. Laboratory examination reveals increased IgE and decreased IgG levels, as well as reduced numbers of circulating CD19+ B-cells including IgM+ naive and class-switched IgG memory B-cells, with a concomitant increase in transitional B-cells, while T-cell numbers and function are normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4639190012 Interleukin 21 related infantile inflammatory bowel disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4639191011 IL21-related infantile inflammatory bowel disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4639192016 Interleukin 21 related infantile inflammatory bowel disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4639193014 A rare autosomal recessive primary immunodeficiency characterised by infancy onset of severe inflammatory bowel disease with life-threatening diarrhoea and failure to thrive, oral aphthous ulcers, and recurrent severe upper and lower respiratory tract infections with finger clubbing. Laboratory examination reveals increased IgE and decreased IgG levels, as well as reduced numbers of circulating CD19+ B-cells including IgM+ naive and class-switched IgG memory B-cells, with a concomitant increase in transitional B-cells, while T-cell numbers and function are normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4639194015 A rare autosomal recessive primary immunodeficiency characterized by infancy onset of severe inflammatory bowel disease with life-threatening diarrhea and failure to thrive, oral aphthous ulcers, and recurrent severe upper and lower respiratory tract infections with finger clubbing. Laboratory examination reveals increased IgE and decreased IgG levels, as well as reduced numbers of circulating CD19+ B-cells including IgM+ naive and class-switched IgG memory B-cells, with a concomitant increase in transitional B-cells, while T-cell numbers and function are normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3397491001000115 IL21-abhängige infantile chronisch-entzündliche Darmerkrankung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6368311000241116 MICI (maladie inflammatoire chronique de l'intestin) liée à l'IL-21 (interleukine 21) chez le bébé de moins d'un an fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6368321000241111 maladie inflammatoire chronique de l'intestin liée à l'interleukine 21 chez le nourrisson fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6368331000241113 MICI (maladie inflammatoire chronique de l'intestin) infantile liée à l'IL-21 (interleukine 21) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6368311000241116 MICI (maladie inflammatoire chronique de l'intestin) liée à l'IL-21 (interleukine 21) chez le bébé de moins d'un an fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6368321000241111 maladie inflammatoire chronique de l'intestin liée à l'interleukine 21 chez le nourrisson fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6368331000241113 MICI (maladie inflammatoire chronique de l'intestin) infantile liée à l'IL-21 (interleukine 21) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3397491001000115 IL21-abhängige infantile chronisch-entzündliche Darmerkrankung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Interleukin 21 related infantile inflammatory bowel disease (disorder) Is a Inflammatory bowel disease is a systemic disorder comprised of two major disorders: ulcerative colitis and Crohn disease. Crohn disease can affect any part of the digestive system while ulcerative colitis is confined to the colon. Both disorders may affect sites outside of the digestive system true Inferred relationship Existential restriction modifier (core metadata concept)
Interleukin 21 related infantile inflammatory bowel disease (disorder) Is a Primary immune deficiency disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Interleukin 21 related infantile inflammatory bowel disease (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Interleukin 21 related infantile inflammatory bowel disease (disorder) Occurrence Infancy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Interleukin 21 related infantile inflammatory bowel disease (disorder) Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Interleukin 21 related infantile inflammatory bowel disease (disorder) Pathological process (attribute) Dysregulated host response (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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