Complement 2 deficiency

disorder

SNOMED 234599007CUI C0398756

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

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

Blood spots

HP:0000979

SLE

HP:0002725

Related Conditions

Classical complement pathway abnormality(parent)

Quick Facts

SNOMED CT: 234599007
UMLS CUI: C0398756
Fully Specified Name: Complement 2 deficiency (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 2

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.