As for other autosomal recessive diseases, the recurrence risk for each subsequent child of the same parents is 25%.

This phenomenon may maintain and possibly even increase the incidence of autosomal recessive disease.

Mutations of the NF2 gene cause a human autosomal dominant disease called neurofibromatosis type 2.

This is known as an autosomal recessive disease.

Hyperekplexia is an extremely rare autosomal dominant neurological disease.

It is classified as an autosomal recessive disease, one that can be passed down through the generations.

It is an autosomal dominant disease with penetrance that is generally accepted to be 80%.

It is a rare, hereditary recessive autosomal disease, in general, diagnosed during childhood.

This syndrome is inherited as an autosomal disease.

It is an autosomal dominant disease, which means a person can get if only one of their parents has the abnormal gene.