KBTBD3
Description
The KBTBD3 (kelch repeat and BTB domain containing 3) is a protein-coding gene located on chromosome 11.
KBTBD3 is also known as BKLHD3.
Associated Diseases
- myeloperoxidase deficiency
- neutropenia, severe congenital, 2, autosomal dominant
- reticular dysgenesis
- nonimmune chronic idiopathic neutropenia of adults
- hereditary neutrophilia
- neutropenia, severe congenital, 1, autosomal dominant
- autosomal recessive severe congenital neutropenia due to CSF3R deficiency
- X-linked sideroblastic anemia 1
- X-linked severe congenital neutropenia
- monosomy 7 myelodysplasia and leukemia syndrome 2
- neutrophil immunodeficiency syndrome
- substance abuse
