User:Sanjana muppavarapu/Genetic disorder

An illness characterized by one or more anomalies in the genome is referred to as a genetic condition. A chromosomal aberration or a mutation One or more genes may have a mutation. Despite the fact that polygenic disorders are more. The expression is frequently used when referring to issues that have a single genetic cause, either in a gene or chromosome. Before embryonic development, the critical mutation may arise naturally, come from two parents who carry the defective gene or be inherited from a parent who already has the condition. It is frequently referred to as a hereditary disease if a genetic abnormality is inherited from either one or both parents. Some diseases have an X-linked inheritance pattern and are brought on by X chromosomal mutations.