CACNA1C-related disorder
MONDO:0700321Any human disease (syndromic or non syndromic) in which the cause of the disease is a variation in the CACNA1C gene.
1 clinical trial for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Timothy syndrome
(1)
Timothy syndrome type 1
(1)
Brugada syndrome 3
(0)
Long QT syndrome 8
(0)
Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures
(0)
Timothy syndrome, atypical type
(0)
Timothy syndrome, classic type
(0)
Timothy syndrome type 2
(0)