Chromosome 10, monosomy 10q (medical condition): A rare disorder caused by the deletion of a portion of chromosome 10q. The range and severity of symptoms is determined by the size of the portion that is deleted.
See also:
Deletion 10q:
»Introduction: Deletion 10q
»Symptoms of Deletion 10q
These medical condition or symptom topics may be relevant to medical information for Chromosome 10, monosomy 10q:
Chromosome 10, monosomy 10q 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, monosomy 10q, or a subtype of Chromosome 10, monosomy 10q,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Chromosome 10, monosomy 10q: Another name for Deletion 10q (or close medical condition association).
»Introduction: Deletion 10q
»Symptoms of Deletion 10q
Some of the symptoms of Chromosome 10, monosomy 10q incude:
See full list of 34 symptoms of Chromosome 10, monosomy 10q (Deletion 10q)
Source - NIH
Search to find out more about Chromosome 10, monosomy 10q:
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