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Chromosome 1, deletion q21 q25: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as retarded fetal growth, osteoporosis, facial anomalies and hearing loss. More detailed information about the symptoms, causes, and treatments of Chromosome 1, deletion q21 q25 is available below.
See full list of 29 symptoms of Chromosome 1, deletion q21 q25
Read more about causes of Chromosome 1, deletion q21 q25.
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Chromosome 1, deletion q21 q25 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, deletion q21 q25, or a subtype of Chromosome 1, deletion q21 q25,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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