Chromosome 10, trisomy 10pter p13 (medical condition): A rare chromosomal disorder where duplication of a portion of chromosome 10 causes various abnormalities such as a wasted build, gut and heart placement abnormalities and lack of reflexes.
See also:
Chromosome 10, trisomy 10pter p13:
»Introduction: Chromosome 10, trisomy 10pter p13
»Symptoms of Chromosome 10, trisomy 10pter p13
These medical condition or symptom topics may be relevant to medical information for Chromosome 10, trisomy 10pter p13:
Chromosome 10, trisomy 10pter p13 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 10, trisomy 10pter p13, or a subtype of Chromosome 10, trisomy 10pter p13,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Chromosome 10, trisomy 10pter p13 (medical condition): See Chromosome 10, trisomy 10pter p13 (disease information).
»Introduction: Chromosome 10, trisomy 10pter p13
»Symptoms of Chromosome 10, trisomy 10pter p13
Source - NIH
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