Recessive is carried by both parents
In simplest terms, the disease is recessive, so two copies of the gene that cause it are necessary. Both parents have only one copy of the gene, so, they don't have it, but are carriers. A child gets half his or her genes from each parent. If the child gets the bad gene from each parent, the child will have the disease. There is a 25% chance of this happening with every child these parents have.
Canavan disease is an autosomal recessive genetic condition
Some movement disorders, including Huntington's disease and inherited ataxias, are caused by inherited genetic defects
WAS is inherited as an X-linked genetic disorder and will therefore only affect males.
There usually is not a genetic limit on strength unless there is a genetic disease or disorder.
Spherocytosis
inherited
Both parents are carriers of the recessive gene and if the child inherits that gene from both mother and father the child will have the disease even though the parents don't.
A disorder you inherit from your ancestors.
colorblindness and hemophilia.
the answer is papaya
by inherited disorder from both or one parent, such as diabetes, cystic fibrosis, parkinsons disease, huntingtons disease etc.
If it is a genetic disease/disorder that means it is a problem in the person's DNA which was created before the birth therefore it is not acquired. Although it can be inherited, it can also have no relation to the family of the offspring whatsoever.
When a genetic disorder is recessive, that means that two copies of the gene are necessary to have the trait or disorder. One is inherited from the mother, and one from the father. Disorders of this type include: cystic fibrosis, sickle cell anemia, and Tay-Sachs disease.
Huntingtons disease is a genetic/inherited diesease. It is caused by a faulty allele (a dominant one), which can be inherited by parents. Spontanoius mutations may also occur which would cause the faulty gene and therefore huntingtons disorder.
yes,it is a genetic disorder
Refsum disease is inherited as an autosomal recessive disorder, which means that two unaffected carrier parents have a 25% chance of having an affected child in every pregnancy.
An acquiring disease is not genetic or inherited. It is a disease acquired by other means.