WDR13
Description
The WDR13 (WD repeat domain 13) is a protein-coding gene located on chromosome X.
WDR13 is also known as MG21.
Associated Diseases
- hyperinsulinemic hypoglycemia, familial, 2
- hypoinsulinemic hypoglycemia and body hemihypertrophy
- hyperinsulinemic hypoglycemia, familial, 1
- obesity due to prohormone convertase I deficiency
- exercise-induced hyperinsulinism
- hyperinsulinism due to INSR deficiency
- hyperinsulinism-hyperammonemia syndrome
- autosomal recessive hyperinsulinism due to Kir6.2 deficiency
- obesity due to pro-opiomelanocortin deficiency
- obesity due to melanocortin 4 receptor deficiency
- pancreatic agenesis 2
- short stature due to primary acid-labile subunit deficiency
- islet cell adenomatosis
- hyperinsulinism due to HNF1A deficiency
- pancreatic agenesis 1
- autosomal dominant hyperinsulinism due to Kir6.2 deficiency
- short stature due to GHSR deficiency
- adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia
