When caused by a mutation in the DNM2 gene, the disorder is autosomal dominant, meaning it can be passed on by one mutated gene.
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When the mutation takes place in the BIN1 gene, the disease is instead autosomal recessive, and both genes must be mutated for the disease to be inherited.
Congenital disorder | Congenital adrenal hyperplasia | X-linked myotubular myopathy | X-linked congenital stationary night blindness | Myopathy | Leber's congenital amaurosis | Congenital lacrimal duct obstruction | Congenital insensitivity to pain with anhidrosis | Congenital fiber type disproportion | congenital disorder | Congenital chloride diarrhea | congenital adrenal hyperplasia |