Tubulinopathy

MONDO:0100153

A nervous system disorder characterized by complex cortical malformations including in most cases dysmorphic basal ganglia and/or corpus callosum in which the cause of the disease is a variation in a tubulin gene.

0 clinical trials for this condition and its sub-types, 0 tagged with Tubulinopathy itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Nervous system disorder (26588)

Sub-types of Tubulinopathy

TUBB3-related tubulinopathy 0 trials
1 sub-type
- Fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement 0 trials
Uner Tan Syndrome 0 trials
Complex cortical dysplasia with other brain malformations 5 0 trials
Tubulinopathy-associated dysgyria 0 trials

Including sub-types (0) Tagged with Tubulinopathy (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.