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Dictionary » Trisomy 13p
 

Trisomy 13p

Introduction: Trisomy 13p

Description of Trisomy 13p

Trisomy 13p (medical condition): A rare chromosomal disorder where duplication of a portion of chromosome...more »

See also:

Chromosome 13p duplication:
  »Introduction: Chromosome 13p duplication
  »Symptoms of Chromosome 13p duplication

Trisomy 13p: Related Topics

These medical condition or symptom topics may be relevant to medical information for Trisomy 13p:

Trisomy 13p: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

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

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 as a Disease

Trisomy 13p: Another name for Chromosome 13p duplication (or close medical condition association).
  »Introduction: Chromosome 13p duplication
  »Symptoms of Chromosome 13p duplication

Trisomy 13p: Related Diseases

Trisomy 13p: Trisomy 13p is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Trisomy 13p (Chromosome 13p duplication)

Some of the symptoms of Trisomy 13p incude:

Trisomy 13p: Related Disease Topics

These medical disease topics may be related to Trisomy 13p:

Terms associated with Trisomy 13p:

Terms Similar to Trisomy 13p:

Source - NIH

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Medical dictionaries:

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