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2p15-16.1 microdeletion syndrome and Chromosome 2

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

Difference between 2p15-16.1 microdeletion syndrome and Chromosome 2

2p15-16.1 microdeletion syndrome vs. Chromosome 2

2p15-16.1 microdeletion is a rare genetic disorder caused by a small deletion in the short arm of human chromosome 2. Chromosome 2 is one of the 23 pairs of chromosomes in humans.

Similarities between 2p15-16.1 microdeletion syndrome and Chromosome 2

2p15-16.1 microdeletion syndrome and Chromosome 2 have 4 things in common (in Unionpedia): Base pair, Gene, Locus (genetics), Pseudogene.

Base pair

A base pair (bp) is a unit consisting of two nucleobases bound to each other by hydrogen bonds.

2p15-16.1 microdeletion syndrome and Base pair · Base pair and Chromosome 2 · See more »

Gene

In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.

2p15-16.1 microdeletion syndrome and Gene · Chromosome 2 and Gene · See more »

Locus (genetics)

A locus (plural loci) in genetics is a fixed position on a chromosome, like the position of a gene or a marker (genetic marker).

2p15-16.1 microdeletion syndrome and Locus (genetics) · Chromosome 2 and Locus (genetics) · See more »

Pseudogene

Pseudogenes are segments of DNA that are related to real genes.

2p15-16.1 microdeletion syndrome and Pseudogene · Chromosome 2 and Pseudogene · See more »

The list above answers the following questions

2p15-16.1 microdeletion syndrome and Chromosome 2 Comparison

2p15-16.1 microdeletion syndrome has 32 relations, while Chromosome 2 has 191. As they have in common 4, the Jaccard index is 1.79% = 4 / (32 + 191).

References

This article shows the relationship between 2p15-16.1 microdeletion syndrome and Chromosome 2. To access each article from which the information was extracted, please visit:

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