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Human genome and Mitochondrial disease

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between Human genome and Mitochondrial disease

Human genome vs. Mitochondrial disease

The human genome is the complete set of nucleic acid sequences for humans, encoded as DNA within the 23 chromosome pairs in cell nuclei and in a small DNA molecule found within individual mitochondria. Mitochondrial diseases are a group of disorders caused by dysfunctional mitochondria, the organelles that generate energy for the cell.

Similarities between Human genome and Mitochondrial disease

Human genome and Mitochondrial disease have 3 things in common (in Unionpedia): Mitochondrial DNA, Mitochondrion, Mutation.

Mitochondrial DNA

Mitochondrial DNA (mtDNA or mDNA) is the DNA located in mitochondria, cellular organelles within eukaryotic cells that convert chemical energy from food into a form that cells can use, adenosine triphosphate (ATP).

Human genome and Mitochondrial DNA · Mitochondrial DNA and Mitochondrial disease · See more »

Mitochondrion

The mitochondrion (plural mitochondria) is a double-membrane-bound organelle found in most eukaryotic organisms.

Human genome and Mitochondrion · Mitochondrial disease and Mitochondrion · See more »

Mutation

In biology, a mutation is the permanent alteration of the nucleotide sequence of the genome of an organism, virus, or extrachromosomal DNA or other genetic elements.

Human genome and Mutation · Mitochondrial disease and Mutation · See more »

The list above answers the following questions

Human genome and Mitochondrial disease Comparison

Human genome has 206 relations, while Mitochondrial disease has 75. As they have in common 3, the Jaccard index is 1.07% = 3 / (206 + 75).

References

This article shows the relationship between Human genome and Mitochondrial disease. To access each article from which the information was extracted, please visit:

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