elliptocytosis 1
Findings
No curated finding names elliptocytosis 1 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any hereditary elliptocytosis in which the cause of the disease is a mutation in the EPB41 gene.
Definition from the Mondo Disease Ontology (MONDO:0012731), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
2 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- ElliptocytosisHPOHP:0004445
- Hemolytic anemiaHPOHP:0001878
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- EPB41HGNC:3377
- Definitive · Ambry Genetics · Semidominant · 2024
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2018
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2018
- Strong · PanelApp Australia · Semidominant · 2025
Where it sits
Other names
4 names
Resolves to: elliptocytosis 1
- Also called
- elliptocytosis type 1elliptocytosis-1EPB41 hereditary elliptocytosishereditary elliptocytosis caused by mutation in EPB41