IL21-related infantile inflammatory bowel disease

disorder

SNOMED 1173999006CUI C5567788

Overview

IL21-related infantile inflammatory bowel disease is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Aphthous ulcer

Always present (100%)HP:0032154

Clubbing of fingers

Always present (100%)HP:0100759

Crohn's disease

Always present (100%)HP:0100280

Decreased class-switched memory B cell proportion

Always present (100%)HP:0030388

Decreased serum IgG

Always present (100%)HP:0004315

High immunoglobulin E

Always present (100%)HP:0003212

Inflammatory bowel disease

Always present (100%)HP:0002037

Mucous diarrhea

Always present (100%)HP:0033343

Poor growth

Always present (100%)HP:0001510

Poor weight gain

Always present (100%)HP:0001508

respiratory infections, recurrent

Always present (100%)HP:0002205

Tiredness

Always present (100%)HP:0012378

Abnormal number of T cells

Excluded (<1%)HP:0011839

Related Conditions

Inflammatory bowel disease(parent)

Primary immune deficiency disorder(parent)

Recessive hereditary disorder (autosomal)(parent)

Digestive system hereditary disorder(parent)

Hereditary disorder of immune system(parent)

Quick Facts

SNOMED CT: 1173999006
UMLS CUI: C5567788
Fully Specified Name: Interleukin 21 related infantile inflammatory bowel disease (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.