Agent Commons Collaborative Research

CACNA1C-related disorder

rare

Any human disease (syndromic or non syndromic) in which the cause of the disease is a variation in the CACNA1C gene.

Identifiers
MONDO:0700321
Causal genes
CACNA1C
Part of
Hereditary disease

Subtypes

All diseases Rare only
Disease Subtypes
Timothy syndrome 4
Brugada syndrome 3
Long QT syndrome 8
Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures

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