Cure My Disease

Don't miss your cure!

Log in / Sign up

Congenital dyserythropoietic anemia

MONDO:0019403

Congenital dyserythropoietic anemia (CDA) is a heterogenous group of hematological disorders of late erythropoiesis and red cell abnormalities that lead to anemia. Five types of CDA are defined: CDA I, CDA II, CDA III, CDA IV and thrombocytopenia with CDA.

Also known as: CDA, anemia, congenital dyserythropoietic, congenital dyshaematopoietic anaemia, congenital dyshaematopoietic anemia, dyserythropoietic anemia, congenital

12 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Sub-types

Congenital dyserythropoietic anemia type 1 (1) Congenital dyserythropoietic anemia type 2 (1) Anemia, congenital dyserythropoietic, type 1a (0) Anemia, congenital dyserythropoietic, type IIIb, autosomal recessive (0) Anemia, congenital dyserythropoietic, type IVb (0) Congenital dyserythropoietic anemia type 3 (0) Congenital dyserythropoietic anemia type 4 (0) Congenital dyserythropoietic anemia type type 1B (0) Pancreatic insufficiency-anemia-hyperostosis syndrome (0) Thrombocytopenia with congenital dyserythropoietic anemia (0) X-linked dyserythropoetic anemia with abnormal platelets and neutropenia (0)

Broader categories

Disease (680) Anemia (233) Hereditary disease (176) Hematologic disorder (170) Hemolytic anemia (19) Human disease (14) Familial hemolytic anemia (3) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0)

Trials to join now! 6 Not yet recruiting 2 Not yet finished but already full! 2 Completed 2