Chromosome 2, monosomy 2p22

Chromosome 2, monosomy 2p22: Introduction

Chromosome 2, monosomy 2p22: A rare chromosomal disorder where deletion of a portion of chromosome 2 causes various abnormalities such as deafness, intestinal problems, mental retardation and speech defects. More detailed information about the symptoms, causes, and treatments of Chromosome 2, monosomy 2p22 is available below.

Symptoms of Chromosome 2, monosomy 2p22

• Hole in the iris
• Conductive deafness
• Epicanthic folds
• Hirschsprung's disease
• Enlarged colon
• more symptoms...»

See full list of 8 symptoms of Chromosome 2, monosomy 2p22

Causes of Chromosome 2, monosomy 2p22

Read more about causes of Chromosome 2, monosomy 2p22.

Disease Topics Related To Chromosome 2, monosomy 2p22

Research the causes of these diseases that are similar to, or related to, Chromosome 2, monosomy 2p22:

• Rare chromosomal disorder
• Epicanthal folds
• Conductive deafness
• Dilated megacolon
• Speech abnormalities
• more related diseases...»

Statistics for Chromosome 2, monosomy 2p22

• Medical statistics for Chromosome 2, monosomy 2p22
• Prevalence and incidence statistics for Chromosome 2, monosomy 2p22
• Death and Mortality statistics for Chromosome 2, monosomy 2p22
• Society statistics for Chromosome 2, monosomy 2p22

Chromosome 2, monosomy 2p22: Broader Related Topics

• Genetic conditions
• more types...»

Types of Chromosome 2, monosomy 2p22

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Definitions of Chromosome 2, monosomy 2p22:

Chromosome 2, monosomy 2p22 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 2, monosomy 2p22, or a subtype of Chromosome 2, monosomy 2p22, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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