familial hemolytic anemia
MONDO:0003689Mondo
Findings
No curated finding names familial hemolytic anemia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.
Definition from the Mondo Disease Ontology (MONDO:0003689), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
- Narrower terms (23)
- abetalipoproteinemia
- congenital dyserythropoietic anemia
- congenital nonspherocytic hemolytic anemia
- cryohydrocytosis
- cutaneous porphyria
- dehydrated hereditary stomatocytosis 2
- dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema
- elliptocytosis 1
- elliptocytosis 2
- familial pseudohyperkalemia
- glycogen storage disease due to aldolase A deficiency
- glycogen storage disease VII
- hemolytic anemia due to diphosphoglycerate mutase deficiency
- hemolytic disease of fetus and newborn, RH-induced
- hereditary cryohydrocytosis with reduced stomatin
- hereditary spherocytosis
- overhydrated hereditary stomatocytosis
- primary CD59 deficiency
- renal tubular acidosis, distal, 4, with hemolytic anemia
- Rh deficiency syndrome
- southeast Asian ovalocytosis
- triosephosphate isomerase deficiency
- X-linked congenital hemolytic anemia
Other names
2 names
Resolves to: familial hemolytic anemia
- Also called
- congenital hemolytic anemiahereditary hemolytic anemia