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CACNA1C-related disorder

MONDO:0700321

Any 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, 0 tagged with CACNA1C-related disorder itself.

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Where it sits in the disease tree

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Part of

↑ Hereditary disease (18235)

Sub-types of CACNA1C-related disorder

Timothy syndrome 1 trial
2 sub-types
- Timothy syndrome, classic type 0 trials · 1 incl. sub-types Sub-types →
- Timothy syndrome, atypical type 0 trials
Brugada syndrome 3 0 trials
Long QT syndrome 8 0 trials
Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures 0 trials

Most studied deeper sub-types

Timothy syndrome type 1 (1) Timothy syndrome type 2 (0)

Including sub-types (1) Tagged with CACNA1C-related disorder (0)

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