Overview
Intestinal lymphangiectasis 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.
Abnormal hair morphology
HP:0001595
Absolute lymphocyte count decrease
HP:0001888
Decreased serum IgG
HP:0004315
Dependant oedema
HP:0010741
Intestinal lymphangiectasia
HP:0002593
Intestinal malabsorption
HP:0002024
Neonatal hypoproteinemia
HP:0008360
Prominent floating ribs
HP:0006641
Soft tissue swelling
HP:0000969
Related Conditions
Primary intestinal lymphangiectasia(child)
Secondary intestinal lymphangiectasia(child)
Aplasia cutis congenita with intestinal lymphangiectasia syndrome(child)
Hennekam lymphangiectasia-lymphoedema syndrome(child)
Disorder of lymphatics(parent)
Soft tissue lesion(parent)
Disorder of abdominopelvic segment of trunk(parent)
Quick Facts
- SNOMED CT
- 197260007
- UMLS CUI
- C0024215
- Fully Specified Name
- Intestinal lymphangiectasis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 9
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.