Faster access than browser!Similarities between Mutation and Wilson's disease
Mutation and Wilson's disease have 10 things in common (in Unionpedia): Amino acid, Arginine, Dominance (genetics), Gene, Genetic testing, Hemoglobin, PRNP, Red blood cell, Superoxide dismutase, Zygosity.
Amino acid
Amino acids are organic compounds containing amine (-NH2) and carboxyl (-COOH) functional groups, along with a side chain (R group) specific to each amino acid.
Amino acid and Mutation · Amino acid and Wilson's disease ·
Arginine
Arginine (symbol Arg or R) is an α-amino acid that is used in the biosynthesis of proteins.
Arginine and Mutation · Arginine and Wilson's disease ·
Dominance (genetics)
Dominance in genetics is a relationship between alleles of one gene, in which the effect on phenotype of one allele masks the contribution of a second allele at the same locus.
Dominance (genetics) and Mutation · Dominance (genetics) and Wilson's disease ·
Gene
In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
Gene and Mutation · Gene and Wilson's disease ·
Genetic testing
Genetic testing, also known as DNA testing, allows the determination of bloodlines and the genetic diagnosis of vulnerabilities to inherited diseases.
Genetic testing and Mutation · Genetic testing and Wilson's disease ·
Hemoglobin
Hemoglobin (American) or haemoglobin (British); abbreviated Hb or Hgb, is the iron-containing oxygen-transport metalloprotein in the red blood cells of all vertebrates (with the exception of the fish family Channichthyidae) as well as the tissues of some invertebrates.
Hemoglobin and Mutation · Hemoglobin and Wilson's disease ·
PRNP
PRNP (PRioN Protein) is the human gene encoding for the major prion protein PrP (for prion protein), also known as CD230 (cluster of differentiation 230).
Mutation and PRNP · PRNP and Wilson's disease ·
Red blood cell
Red blood cells-- also known as RBCs, red cells, red blood corpuscles, haematids, erythroid cells or erythrocytes (from Greek erythros for "red" and kytos for "hollow vessel", with -cyte translated as "cell" in modern usage), are the most common type of blood cell and the vertebrate's principal means of delivering oxygen (O2) to the body tissues—via blood flow through the circulatory system.
Mutation and Red blood cell · Red blood cell and Wilson's disease ·
Superoxide dismutase
Superoxide dismutase (SOD) is an enzyme that alternately catalyzes the dismutation (or partitioning) of the superoxide (O2&minus) radical into either ordinary molecular oxygen (O2) or hydrogen peroxide (H2O2).
Mutation and Superoxide dismutase · Superoxide dismutase and Wilson's disease ·
Zygosity
Zygosity is the degree of similarity of the alleles for a trait in an organism.
The list above answers the following questions
- What Mutation and Wilson's disease have in common
- What are the similarities between Mutation and Wilson's disease
Mutation and Wilson's disease Comparison
Mutation has 296 relations, while Wilson's disease has 176. As they have in common 10, the Jaccard index is 2.12% = 10 / (296 + 176).
References
This article shows the relationship between Mutation and Wilson's disease. To access each article from which the information was extracted, please visit:
