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Chromosome 1, monosomy 1p31 p22: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as mental retardation, missing teeth and small eyes and jaw. More detailed information about the symptoms, causes, and treatments of Chromosome 1, monosomy 1p31 p22 is available below.
See full list of 14 symptoms of Chromosome 1, monosomy 1p31 p22
Read more about causes of Chromosome 1, monosomy 1p31 p22.
Research the causes of these diseases that are similar to, or related to, Chromosome 1, monosomy 1p31 p22:
See full list of 17 occasional symptoms of Chromosome 1, monosomy 1p31 p22
Types of Chromosome 1, monosomy 1p31 p22
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Chromosome 1, monosomy 1p31 p22 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 1, monosomy 1p31 p22, or a subtype of Chromosome 1, monosomy 1p31 p22,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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