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familial hemolytic anemia

GWAS Targets (0)
 No GWAS traits found
Disease Hierarchy
Parents
Mendelian disease (13361)
Tbio

8932

Tdark

2157

Tchem

1652

Tclin

620

hemolytic anemia (99)
Tbio

61

Tchem

23

Tclin

15

Children
constitutional hemolytic anemia due to membrane defect (30)
Tbio

19

Tclin

6

Tchem

5

hemolytic-uremic syndrome (22)
Tbio

14

Tclin

4

Tchem

4

congenital dyserythropoietic anemia (9)
Tbio

9

congenital nonspherocytic hemolytic anemia (6)
Tbio

4

Tchem

2

cutaneous porphyria (4)
Tbio

4

Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome (3)
Tbio

3

inherited paroxysmal nocturnal hemoglobinuria (2)
Tbio

2

hemolytic anemia due to diphosphoglycerate mutase deficiency (1)
Tbio

1

gamma-glutamylcysteine synthetase deficiency (1)
Tchem

1

glycogen storage disease VII (1)
Tbio

1

non-spherocytic hemolytic anemia due to hexokinase deficiency (1)
Tchem

1

Norum disease (1)
Tchem

1

hemolytic anemia due to pyrimidine 5' nucleotidase deficiency (1)
Tbio

1

glycogen storage disease due to phosphoglycerate kinase 1 deficiency (1)
Tchem

1

glycogen storage disease due to aldolase A deficiency (1)
Tbio

1

hemolytic anemia due to adenylate kinase deficiency (1)
Tbio

1

triosephosphate isomerase deficiency (1)
Tbio

1

STAT3-related early-onset multisystem autoimmune disease (1)
Tchem

1

inherited glutathione synthetase deficiency (1)
Tbio

1

X-linked congenital hemolytic anemia (1)
Tbio

1

hemolytic anemia due to erythrocyte adenosine deaminase overproduction (0)
Target Novelty (Tin-x)