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Factor I deficiency

disorder
SNOMED 234621005CUI C3463916

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.

Decreased serum complement factor I
Always present (100%)HP:0005356
Decreased serum complement C3 level
Frequent (30-79%)HP:0005421
Decreased serum complement factor B
Frequent (30-79%)HP:0005416
Infected joint
Frequent (30-79%)HP:0003095
Recurrent meningitis
Frequent (30-79%)HP:0006946
Recurrent meningococcal disease
Frequent (30-79%)HP:0005381
Recurrent middle ear infection
Frequent (30-79%)HP:0000403
Recurrent sinus infections
Frequent (30-79%)HP:0011108
Decreased serum complement factor H
HP:0005369
Glomerulonephritis
HP:0000099
Inflammation of blood vessel
HP:0002633
Pyelonephritis
HP:0012330
Recurrent H. influenzae infections
HP:0005376
Recurrent streptococcus pneumoniae infections
HP:0005366
Renal failure in adulthood
HP:0000083
Repeated bladder infections
HP:0000010
Skin infections, recurrent
HP:0001581

Quick Facts

SNOMED CT
234621005
UMLS CUI
C3463916
Fully Specified Name
Factor I deficiency (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
17
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.