DCDC2B
Description
The DCDC2B (doublecortin domain containing 2B) is a protein-coding gene located on chromosome 1.
DCDC2B is also known as -.
Associated Diseases
- primary familial polycythemia due to EPO receptor mutation
- erythrocytosis, familial, 3
- erythrocytosis, familial, 6
- hemolytic anemia due to diphosphoglycerate mutase deficiency
- alpha thalassemia-intellectual disability syndrome type 1
- erythrocytosis, familial, 4
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- hemolytic anemia due to adenylate kinase deficiency
- Heinz body anemia
- X-linked sideroblastic anemia 1
- delta-beta-thalassemia
- hemoglobin E-beta-thalassemia syndrome
- familial isolated congenital asplenia
- hemoglobin C-beta-thalassemia syndrome
- hemoglobin D disease
- hemolytic anemia due to erythrocyte adenosine deaminase overproduction
- dehydrated hereditary stomatocytosis
- dominant beta-thalassemia
