FAM110B
Description
The FAM110B (family with sequence similarity 110 member B) is a protein-coding gene located on chromosome 8.
FAM110B is also known as C8orf72.
Associated Diseases
- primary familial polycythemia due to EPO receptor mutation
- hemolytic anemia due to diphosphoglycerate mutase deficiency
- erythrocytosis, familial, 3
- erythrocytosis, familial, 6
- dehydrated hereditary stomatocytosis
- erythrocytosis, familial, 4
- hemolytic anemia due to erythrocyte adenosine deaminase overproduction
- X-linked sideroblastic anemia 1
- Rh deficiency syndrome
- elliptocytosis 2
- cryohydrocytosis
- overhydrated hereditary stomatocytosis
