Treatments & Interventions
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Autoimmune haemolytic anemia
HP:0001890
Laboratory abnormality
HP:0001939
Related Conditions
Primary (idiopathic) autoimmune hemolytic anemia(child)
Secondary autoimmune hemolytic anemia(child)
Paroxysmal cold hemoglobinuria(child)
Autoimmune hemolytic anemia, categorized by antibody class AND/OR complement(child)
Hemolytic anemia due to warm antibody(child)
Primary cold-type hemolytic anemia(child)
Secondary cold-type hemolytic anemia(child)
Cold autoimmune haemolytic anaemia(child)
Maternal autoimmune hemolytic anemia(child)
Drug-induced autoimmune hemolytic anemia(child)
Neonatal autoimmune haemolytic anaemia(child)
Lymphocyte passenger syndrome following organ transplantation(child)
Autoimmune disease(parent)
Antibody-mediated anemia(parent)
Acquired hemolytic anemia(parent)
Quick Facts
- SNOMED CT
- 413603009
- UMLS CUI
- C0002880
- Fully Specified Name
- Autoimmune hemolytic anemia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 2
- Known Treatments
- 3
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.