Overview
ALECT2 amyloidosis 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.
Hepatic amyloidosis
Very frequent (80-99%)HP:0012280
Renal amyloidosis
Very frequent (80-99%)HP:0001917
High blood pressure
Frequent (30-79%)HP:0000822
Increased creatinine
Frequent (30-79%)HP:0003259
Proteinuria
Frequent (30-79%)HP:0000093
Pulmonary amyloidosis
Frequent (30-79%)HP:0033247
Renal failure
Frequent (30-79%)HP:0000083
Abnormality of multiple cell lineages in the bone marrow
Occasional (5-29%)HP:0012145
Increased liver function tests
Occasional (5-29%)HP:0002910
Thyroid gland amyloidosis
Occasional (5-29%)HP:6000815
Thyroid goiter
Occasional (5-29%)HP:0000853
Microhematuria
Very rare (1-4%)HP:0002907
Quick Facts
- SNOMED CT
- 1228881003
- UMLS CUI
- C5680047
- Fully Specified Name
- Leukocyte chemotactic factor-2 amyloidosis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 12
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.