A retinopathy caused by biallelic variants in the CNGB3 gene.
Comprehensive, easy-to-understand information about this condition
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Meniere disease
MONDO:0007972
myotonia congenita, autosomal dominant
MONDO:0008055
Andersen-Tawil syndrome
MONDO:0008222
Morvan syndrome
MONDO:0008718
Thomsen and Becker disease
MONDO:0009710
myotonia congenita, autosomal recessive
MONDO:0009715