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Chromosome 3, monosomy 3q13: A rare chromosomal disorder characterized by a range of abnormalities including facial anomalies, kidney dysfunction, large head, small penis and impaired joint mobility. More detailed information about the symptoms, causes, and treatments of Chromosome 3, monosomy 3q13 is available below.
See full list of 18 symptoms of Chromosome 3, monosomy 3q13
Read more about causes of Chromosome 3, monosomy 3q13.
Research the causes of these diseases that are similar to, or related to, Chromosome 3, monosomy 3q13:
Types of Chromosome 3, monosomy 3q13
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Chromosome 3, monosomy 3q13 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 3, monosomy 3q13, or a subtype of Chromosome 3, monosomy 3q13,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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