Chromosome 2, monosomy 2q37

Chromosome 2, monosomy 2q37: Introduction

Chromosome 2, monosomy 2q37: A very rare chromosomal disorder where a part of the long arm of chromosome 2 is missing which results in various birth defects and abnormalities. The features of the disorder are determined by the exact size and location of the deletion. More detailed information about the symptoms, causes, and treatments of Chromosome 2, monosomy 2q37 is available below.

Symptoms of Chromosome 2, monosomy 2q37

• Developmental delay
• Mental retardation
• Seizures
• Distinctive facial features
• Short fingers
• more symptoms...»

See full list of 26 symptoms of Chromosome 2, monosomy 2q37

Causes of Chromosome 2, monosomy 2q37

Read more about causes of Chromosome 2, monosomy 2q37.

Less Common Symptoms of Chromosome 2, monosomy 2q37

• Kidney anomalies
• Genital anomalies
• Wilms tumor
• more symptoms...»

Read more about symptoms of Chromosome 2, monosomy 2q37

Statistics for Chromosome 2, monosomy 2q37

• Medical statistics for Chromosome 2, monosomy 2q37
• Prevalence and incidence statistics for Chromosome 2, monosomy 2q37
• Death and Mortality statistics for Chromosome 2, monosomy 2q37
• Society statistics for Chromosome 2, monosomy 2q37

Chromosome 2, monosomy 2q37: Broader Related Topics

• Genetic conditions
• more types...»

Types of Chromosome 2, monosomy 2q37

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Definitions of Chromosome 2, monosomy 2q37:

Chromosome 2, monosomy 2q37 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 2q37, or a subtype of Chromosome 2, monosomy 2q37, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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