Omodysplasia 1 (OMOD1)

Alias:

Autosomal Recessive Omodysplasia

Micromelic Dysplasia-Dislocation of Radius Syndrome

Omodysplasia Type 1

Omod1

Micromelic Dysplasia, Congenital, with Dislocation of Radius

Micromelic Dysplasia Congenital with Dislocation of Radius

Omodysplasia, Autosomal Recessive

Omodysplasia Autosomal Recessive

Omodysplasia, Generalized Form

Omodysplasia Generalized Form

Omodysplasia, Type 1

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Omodysplasia 1, also known as autosomal recessive omodysplasia, is related to omodysplasia and omodysplasia 2. An important gene associated with Omodysplasia 1 is GPC6 (Glypican 6), and among its related pathways/superpathways are ncRNAs involved in Wnt signaling in hepatocellular carcinoma and mTOR Signaling. Affiliated tissues include bone and heart, and related phenotypes are frontal bossing and depressed nasal bridge

Related ID：

MALACARDS：OMD001

OMIM：258315

MESH：C537746