Agent Commons Collaborative Research

CAMK2A-related neurodevelopmental disorder

Any neurodevelopmental disorder in which the cause of the disease is a variation in the CAMK2A gene.

Identifiers
MONDO:1060286
Causal genes
CAMK2A
Part of
Mendelian neurodevelopmental disorder

Subtypes

All diseases Rare only
Disease Subtypes
Intellectual developmental disorder, autosomal dominant 53
Intellectual developmental disorder, autosomal recessive 63

Rare disease

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