Wolfram-Like Syndrome, Autosomal Dominant (WFSL)

Alias:

Wolfram-Like Syndrome

Wfsl

Hearing Loss, Progressive, with Optic Atrophy and/or Impaired Glucose Regulation

Hearing Loss Progressive with Optic Atrophy and/or Impaired Glucose Regulation

Wolfram-Like Syndrome Autosomal Dominant

Wolfram Syndrome-Like Disease

Wolfram-Like Disorder

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Wolfram-Like Syndrome, Autosomal Dominant, also known as wolfram-like syndrome, is related to wolfram syndrome 1 and 3-methylglutaconic aciduria, type iii. An important gene associated with Wolfram-Like Syndrome, Autosomal Dominant is WFS1 (Wolframin ER Transmembrane Glycoprotein). Affiliated tissues include eye and kidney, and related phenotypes are depression and diabetes mellitus

Related ID：

MALACARDS：WLF011

OMIM：614296

MESH：D014929