Rare diseases · Sign or symptom
Autoimmune hemolytic anemia
HP:0001890
What it means
An autoimmune form of hemolytic anemia.
Rare diseases that can present with this20
Very common80–99%
6Common30–79%
6- Atypical/leaky severe combined immunodeficiency due to partial RAG defect
- Autoimmune lymphoproliferative syndrome
- Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency
- Purine nucleoside phosphorylase deficiency
- STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome
- T-B-NK+ severe combined immunodeficiency due to DCLRE1C deficiency
Sometimes5–29%
5The range is how often this sign appears among people diagnosed with each disease — it is not a probability of having any of them. Many of these signs also occur in common, non-rare conditions. A sign on this page is a conversation to have with a clinician, not a conclusion.
Part of the broader category
Also called: Autoimmune haemolytic anaemia · Autoimmune haemolytic anemia · Autoimmune hemolytic anaemia · Hemolytic anemia, autoimmune
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Start free with EleplanThis page uses the Human Phenotype Ontology (2026-06-23) — Human Phenotype Ontology Consortium, hpo.jax.org. Disease associations from Orphanet (INSERM), CC BY 4.0. Content is educational and is not medical advice.