FAM184B
Description
The FAM184B (family with sequence similarity 184 member B) is a protein-coding gene located on chromosome 4.
FAM184B is also known as -.
Associated Diseases
- diabetes mellitus, permanent neonatal 4
- hypoparathyroidism, familial isolated, 2
- diabetes mellitus, transient neonatal, 3
- permanent neonatal diabetes mellitus 1
- glycogen storage disorder due to hepatic glycogen synthase deficiency
- familial isolated hyperparathyroidism
- adamantinoma
