
Autosome - Wikipedia
An autosome is any chromosome that is not a sex chromosome. [1] . The members of an autosome pair in a diploid cell have the same morphology, unlike those in allosomal (sex …
Autosomal DNA: Definition, Dominant, Recessive, Test, Examples - Healthline
Jun 6, 2019 · Autosomes, or autosomal DNA, make up 22 pairs of chromosomes in your body. Small variations in these genes determine your genetic makeup and whether you inherit …
What Is an Autosomal Chromosome & How Are Traits Inherited?
Aug 18, 2025 · Understand autosomal chromosomes: how they govern the inheritance of traits and contribute to genetic conditions.
Autosomal Dominant & Autosomal Recessive Disorders - Cleveland Clinic
Autosomal means that a specific gene is not on a sex chromosome and is a numbered chromosome. Humans have 46 total chromosomes. Each of your parents gives you 23 …
Autosomal Dominant Disorder
1 day ago · “Autosomal” means that the gene in question is located on one of the numbered, or non-sex, chromosomes. “Dominant” means that a single copy of the mutated gene (from one …
What is Autosomal DNA? - FamilyTreeDNA Blog
Apr 18, 2024 · Autosomal DNA is comprised of the 22 pairs of autosomes (chromosomes 1-22) that you inherit from your parents. Most autosomal DNA tests also include the X chromosome. …
Autosome | Definition & Facts | Britannica
Autosomes differ from sex chromosomes, which make up the 23rd pair of chromosomes in all normal human cells and come in two forms, called X and Y. Autosomes control the inheritance …
Definition of autosomal - NCI Dictionary of Genetics Terms
autosomal (AW-toh-SOH-mul) Having to do with any of the 22 numbered pairs of chromosomes found in most human cells. Autosomal chromosomes are numbered 1-22. The sex …
AUTOSOMAL Definition & Meaning - Merriam-Webster
The meaning of AUTOSOMAL is of, belonging to, located on, or transmitted by an autosome. How to use autosomal in a sentence.
Autosomal inheritance: Dominant vs. recessive disorders
Mar 6, 2023 · In autosomal inheritance, a copy of a faulty gene from one parent can cause a condition in the child. The child will have 50% chance of inheriting the faulty gene.