IGLON5
Description
The IGLON5 (IgLON family member 5) is a protein-coding gene located on chromosome 19.
IGLON5 is also known as -.
Associated Diseases
- Senior-Boichis syndrome
- hepatorenocardiac degenerative fibrosis
- immunodeficiency 75
- nephronophthisis
- renal-hepatic-pancreatic dysplasia 1
- neutropenia, severe congenital, 9, autosomal dominant
- progressive familial intrahepatic cholestasis type 3
- dominant beta-thalassemia
- hemoglobin H disease
