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Trisomy Xpter Xq13 (medical condition): A condition characterised by the duplication of the long arm of chromosome X....more »
These medical condition or symptom topics may be relevant to medical information for Trisomy Xpter Xq13:
Trisomy Xpter Xq13 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Trisomy Xpter Xq13, or a subtype of Trisomy Xpter Xq13,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Trisomy Xpter Xq13 as a "rare disease".
Source - Orphanet
Trisomy Xpter Xq13: Another name for X chromosome, trisomy Xpter Xq13 (or close medical condition association).
»Introduction: X chromosome, trisomy Xpter Xq13
»Symptoms of X chromosome, trisomy Xpter Xq13
Trisomy Xpter Xq13: Trisomy Xpter Xq13 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Trisomy Xpter Xq13 incude:
These medical disease topics may be related to Trisomy Xpter Xq13:
Source - NIH
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