About The Medical Condition Human Genomes
Find the definition of the medical term Human Genomes. Human Genomes defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.
Human Genomes
| Human Genomes Medical Condition |
|---|
What's The Definition Of The Medical Condition Human Genomes?
The complete gene complement contained in a set of chromosomes in a human, either haploid (the set derived from one parent) or diploid (the double set, derived from both parents). The haploid set contains 50,000 to 100,000 genes and about 3 billion base pairs.
|
More Medical Conditions
A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z
Medical Conditions Definitions Of The Day
- Salamandridae ‐ A family of Urodela consisting of 15 living genera and about…
- Industry, Healthcare ‐ Economic sector concerned with the provision, distribution, and…
- Acquired Facial Neuropathy ‐ Diseases of the facial nerve or nuclei. Pontine disorders may…
- Neoplasms, Basal Cell ‐ Neoplasms composed of cells from the deepest layer of the epidermis.…
- Abdominal Pain ‐ Sensation of discomfort, distress, or agony in the abdominal…
- Meningitis, Meningococcic ‐ A fulminant infection of the meninges and subarachnoid fluid…
- Calcium Channel, R-Type ‐ CALCIUM CHANNELS located in the neurons of the brain. They are…
- Gla Protein, Bone ‐ Vitamin K-dependent calcium-binding protein synthesized by osteoblasts…
- Photosensitive Epilepsies ‐ A subtype of epilepsy characterized by seizures that are consistently…
- Diiodotyrosine Receptors ‐ Proteins, usually found in the nucleus, that specifically bind…