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Medical > Human genome

cis configuration

Medical; Human genome

1) Term which indicates that an individual who is heterozygous at two neighboring loci has the two mutations in question on the same chromosome. 3) Characterized by having ...

chimerism

Medical; Human genome

The occurrence in an individual of two or more cell populations of different chromosomal constitutions, derived from different individuals. This contrasts with mosaicism in which ...

collecting tubule

Medical; Human genome

A nonsecretory tubule that receives urine from several nephrons and discharges it into the pelvis of the kidney—called also collecting duct.

conductive hearing loss

Medical; Human genome

10 Involves lesions of the external and middle ear resulting in malconduction of airborne sound. 2) Hearing loss due to interference with the mechanical reception or ...

coding region

Medical; Human genome

Sequence of DNA consisting of a series of nucleotide bases (code) giving rise to the mature messenger RNA that will be translated into the specific amino acids of the protein ...

colitis

Medical; Human genome

1) Inflammation of the colon section of the large intestine, usually with symptoms such as diarrhea (often with blood and mucus), abdominal pain, and fever. 2) Inflammation of ...

connexin

Medical; Human genome

A group of homologous proteins which form the intermembrane channels of gap junctions. The connexins are the products of an identified gene family which has both highly conserved ...