CASK-related intellectual disability

MONDO:1060192

A syndromic disorder in which the cause of the disease is a variation in the CASK gene. It is associated with a wide phenotypic spectrum ranging from mild-to-severe intellectual disability with or without nystagmus to moderate-to-profound intellectual disability and progressive microcephaly with pontine and cerebellar hypoplasia, often associated with seizures.

Also known as: CASK-related disorder

0 clinical trials for this condition and its sub-types, 0 tagged with CASK-related intellectual disability itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ X-linked syndromic intellectual disability (12)

Sub-types of CASK-related intellectual disability

FG syndrome 4 0 trials
X-linked intellectual disability with or without nystagmus 0 trials
Syndromic X-linked intellectual disability Najm type 0 trials

Including sub-types (0) Tagged with CASK-related intellectual disability (0)

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