Congenital anemia

MONDO:0000577

Anemia, the cause of which is present at birth.

Also known as: congenital anaemia (disease), congenital anemia, congenital anemia (disease)

67 clinical trials for this condition and its sub-types, 0 tagged with Congenital anemia itself.

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Where it sits in the disease tree

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Part of

↑ Anemia (975) ↑ Congenital hematological disorder (101)

Sub-types of Congenital anemia

Fanconi anemia 29 trials · 42 incl. sub-types
22 sub-types
- Fanconi anemia complementation group D1 6 trials
- Fanconi anemia complementation group A 4 trials
- Fanconi anemia complementation group E 4 trials
- Fanconi anemia complementation group N 2 trials
- Fanconi anemia, complementation group S 2 trials
- Fanconi anemia complementation group B 0 trials
- Fanconi anemia complementation group C 0 trials
- Fanconi anemia complementation group D2 0 trials
- Fanconi anemia complementation group F 0 trials
- Fanconi anemia complementation group G 0 trials
- Fanconi anemia complementation group I 0 trials
- Fanconi anemia complementation group J 0 trials
- Fanconi anemia complementation group L 0 trials
- Fanconi anemia complementation group O 0 trials
- Fanconi anemia complementation group P 0 trials
- Fanconi anemia complementation group Q 0 trials
- Fanconi anemia complementation group R 0 trials
- Fanconi anemia complementation group T 0 trials
- Fanconi anemia complementation group U 0 trials
- Fanconi anemia complementation group V 0 trials
- Fanconi anemia, complementation group W 0 trials
- Fanconi anemia, complementation group 10 0 trials
Congenital nonspherocytic hemolytic anemia 1 trial · 12 incl. sub-types
10 sub-types
- Pyruvate kinase deficiency of red cells 10 trials
- Anemia, nonspherocytic hemolytic 0 trials · 2 incl. sub-types Sub-types →
- Hemolytic anemia due to adenylate kinase deficiency 1 trial
- Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency 1 trial
- Gamma-glutamylcysteine synthetase deficiency 0 trials
- Glutathione synthetase deficiency without 5-oxoprolinuria 0 trials
- Hemolytic anemia due to erythrocyte adenosine deaminase overproduction 0 trials
- Hemolytic anemia due to glucophosphate isomerase deficiency 0 trials
- Hemolytic anemia due to glutathione reductase deficiency 0 trials
- Non-spherocytic hemolytic anemia due to hexokinase deficiency 0 trials
Myopathy, lactic acidosis, and sideroblastic anemia 3 trials
3 sub-types
- Myopathy, lactic acidosis, and sideroblastic anemia 1 0 trials
- Myopathy, lactic acidosis, and sideroblastic anemia 2 0 trials
- Myopathy, lactic acidosis, and sideroblastic anemia 3 0 trials
Congenital dyserythropoietic anemia type 1 1 trial
2 sub-types
- Anemia, congenital dyserythropoietic, type 1a 0 trials
- Congenital dyserythropoietic anemia type type 1B 0 trials
Congenital dyserythropoietic anemia type 2 1 trial
Congenital dyserythropoietic anemia type 3 0 trials
Congenital dyserythropoietic anemia type 4 0 trials
Severe congenital hypochromic anemia with ringed sideroblasts 0 trials

Most studied deeper sub-types

Anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane (1) Anemia, nonspherocytic hemolytic, due to G6PD deficiency (1) Anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism (0)

Including sub-types (67) Tagged with Congenital anemia (0)

Trials to join now! 27 Not yet recruiting 10 Not yet finished but already full! 20 Completed 8 Terminated 2

Congenital anemia

Where it sits in the disease tree

Most studied deeper sub-types

Gene therapy aims to fix bone marrow failure in fanconi anemia

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