Familial hemolytic anemia
MONDO:0003689A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.
Also known as: congenital hemolytic anemia, hereditary hemolytic anemia, anaemia hemolytic congenital, anemia hemolytic congenital
66 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Pyruvate kinase deficiency of red cells
(10)
Congenital dyserythropoietic anemia
(4)
Abetalipoproteinemia
(2)
Cutaneous porphyria
(2)
Hereditary spherocytosis
(2)
Southeast Asian ovalocytosis
(2)
Anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane
(1)
Anemia, nonspherocytic hemolytic, due to G6PD deficiency
(1)
Congenital dyserythropoietic anemia type 1
(1)
Congenital dyserythropoietic anemia type 2
(1)
Congenital nonspherocytic hemolytic anemia
(1)
Glycogen storage disease due to aldolase A deficiency
(1)
Glycogen storage disease VII
(1)
Hemolytic anemia due to adenylate kinase deficiency
(1)
Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency
(1)
Anemia, congenital dyserythropoietic, type 1a
(0)
Anemia, congenital dyserythropoietic, type IIIb, autosomal recessive
(0)
Anemia, congenital dyserythropoietic, type IVb
(0)
Anemia, nonspherocytic hemolytic
(0)
Anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism
(0)