Robinow Syndrome, Autosomal Dominant 1 (DRS1)

Alias:

Autosomal Dominant Robinow Syndrome 1

Drs1

Acral Dysostosis with Facial and Genital Abnormalities

Fetal Face Syndrome

Robinow Dwarfism

Dysostosis Acral with Facial and Genital Abnormalities

Robinow, Autosomal Dominant Syndrome, Type 1

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Robinow Syndrome, Autosomal Dominant 1, also known as autosomal dominant robinow syndrome 1, is related to autosomal dominant robinow syndrome and robinow syndrome. An important gene associated with Robinow Syndrome, Autosomal Dominant 1 is WNT5A (Wnt Family Member 5A), and among its related pathways/superpathways are Signaling by WNT and Pleural mesothelioma. Affiliated tissues include tongue and heart, and related phenotypes are short nose and short stature

Related ID：

MALACARDS：RBN018

OMIM：180700

MESH：D004392