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Up to: Hereditary disease · Hemolytic anemia

Familial hemolytic anemia

A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.

4 trials tagged with this condition →

Congenital nonspherocytic hemolytic anemia 1 trial · 12 incl. sub-types Sub-types →
Congenital dyserythropoietic anemia 4 trials · 5 incl. sub-types Sub-types →
Abetalipoproteinemia 2 trials
Cutaneous porphyria 2 trials
Hereditary spherocytosis 2 trials Sub-types →
Southeast Asian ovalocytosis 2 trials
Glycogen storage disease VII 1 trial
Glycogen storage disease due to aldolase A deficiency 1 trial
Rh deficiency syndrome 0 trials
X-linked congenital hemolytic anemia 0 trials
Cryohydrocytosis 0 trials
Dehydrated hereditary stomatocytosis 2 0 trials
Dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema 0 trials
Elliptocytosis 1 0 trials
Elliptocytosis 2 0 trials
Familial pseudohyperkalemia 0 trials
Hemolytic anemia due to diphosphoglycerate mutase deficiency 0 trials
Hemolytic disease of fetus and newborn, RH-induced 0 trials
Hereditary cryohydrocytosis with reduced stomatin 0 trials
Overhydrated hereditary stomatocytosis 0 trials
Primary CD59 deficiency 0 trials
Renal tubular acidosis, distal, 4, with hemolytic anemia 0 trials
Triosephosphate isomerase deficiency 0 trials