autosomal recessive disorder

It is an autosomal recessive disorder that can be passed to a child from the parents.

Type 1 Gaucher disease is an autosomal recessive disorder one gets from both parents.

This disease is inherited as an autosomal recessive disorder.

Blue diaper syndrome is thought to be inherited as an autosomal recessive disorder.

Fucosidosis is an autosomal recessive disorder that affects many areas of the body.

Genetically, it is an autosomal recessive disorder, making its occurrence fairly rare.

Like most autosomal recessive disorders, when both parents are carriers, there is a 25% chance for each child to inherit the disease.

The mice are born at the expected Mendelian frequencies for an autosomal recessive disorder.

The parents of a child with an autosomal recessive disorder are usually not affected by the disorder.

Three autosomal recessive disorders involve the inability to metabolize fructose.

Sclerosteosis is an autosomal recessive disorder characterized by bone overgrowth.

It is an autosomal recessive disorder thought to be caused by abnormal development of photoreceptor cells.

Although it is an autosomal recessive disorder, heterozygotes may still manifest much attenuated symptoms.

This autosomal recessive disorder results in a totally non-functional insulin receptor.

Bloom syndrome (BS) is a very rare autosomal recessive disorder.

There are also autosomal recessive disorders that resemble sporadic cases of HD.

However, in recent years, a novel early-onset autosomal recessive disorder was described in this breed.

There are approximately nine different types of oculocutaneous albinism, which is mostly an autosomal recessive disorder.

It is an autosomal recessive disorder, meaning that only individuals inheriting the defective gene from both parents are affected.

Two copies of the gene must be mutated for a person to be affected by an autosomal recessive disorder.

It is a rare, ciliopathic, autosomal recessive disorder characterized by nephronophthisis and progressive eye disease.

Therefore, each parent of an individual with an autosomal recessive disorder has at least one defective copy of the gene.

Serkal syndrome is an autosomal recessive disorder in XX humans.

- Fucosidosis is an autosomal recessive disorder (Both copies of the gene in the must have the mutation).

Typically, people who are carriers of an autosomal recessive disorder do not show symptoms of the disorder.