LCA5L
Description
The LCA5L (lebercilin LCA5 like) is a protein-coding gene located on chromosome 21.
LCA5L is also known as C21orf13.
Associated Diseases
- dehydrated hereditary stomatocytosis
- Rh deficiency syndrome
- gluthathione peroxidase deficiency
- hemoglobin D disease
- hemoglobin E-beta-thalassemia syndrome
- hemolytic anemia due to erythrocyte adenosine deaminase overproduction
- retinitis pigmentosa and erythrocytic microcytosis
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- hemolytic anemia due to glutathione reductase deficiency
- primary familial polycythemia due to EPO receptor mutation
- megaloblastic anemia, folate-responsive
- elliptocytosis 2
- beta-thalassemia-X-linked thrombocytopenia syndrome
