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Trisomy 13p (medical condition): A rare chromosomal disorder where duplication of a portion of chromosome...more »
These medical condition or symptom topics may be relevant to medical information for Trisomy 13p:
Trisomy 13p is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Trisomy 13p, or a subtype of Trisomy 13p,
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 13p as a "rare disease".
Source - Orphanet
Trisomy 13p: Trisomy 13p is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Trisomy 13p incude:
These medical disease topics may be related to Trisomy 13p:
Source - NIH
Search to find out more about Trisomy 13p:
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