LYPD2
Description
The LYPD2 (LY6/PLAUR domain containing 2) is a protein-coding gene located on chromosome 8.
LYPD2 is also known as LYPDC2, UNQ430.
Associated Diseases
- X-linked severe congenital neutropenia
- thrombocytopenia 4
- neutrophil immunodeficiency syndrome
- beta-thalassemia-X-linked thrombocytopenia syndrome
- nonimmune chronic idiopathic neutropenia of adults
- X-linked sideroblastic anemia 1
- thrombocytopenia 2
- DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome
- neutropenia, severe congenital, 2, autosomal dominant
- macrothrombocytopenia, isolated, 2, autosomal dominant
- neutropenia, severe congenital, 1, autosomal dominant
- myeloperoxidase deficiency
- platelet-type bleeding disorder 10
- autosomal recessive severe congenital neutropenia due to CSF3R deficiency
- thrombocytopenia 7
- platelet-type bleeding disorder 15
- neutropenia-monocytopenia-deafness syndrome
