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Dictionary » Monosomy 10pter
 

Monosomy 10pter

Introduction: Monosomy 10pter

Description of Monosomy 10pter

Monosomy 10pter (medical condition): A very rare syndrome caused by a chromosomal defect (10p...more »

See also:

Chromosome 10p terminal deletion syndrome:
  »Introduction: Chromosome 10p terminal deletion syndrome
  »Symptoms of Chromosome 10p terminal deletion syndrome

Monosomy 10pter: Related Topics

These medical condition or symptom topics may be relevant to medical information for Monosomy 10pter:

Monosomy 10pter: Rare Disease

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

Monosomy 10pter is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Monosomy 10pter, or a subtype of Monosomy 10pter, 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 Monosomy 10pter as a "rare disease".

Source - Orphanet

Monosomy 10pter as a Disease

Monosomy 10pter: Another name for Chromosome 10p terminal deletion syndrome (or close medical condition association).
  »Introduction: Chromosome 10p terminal deletion syndrome
  »Symptoms of Chromosome 10p terminal deletion syndrome

Monosomy 10pter: Related Diseases

Monosomy 10pter: Monosomy 10pter is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Monosomy 10pter (Chromosome 10p terminal deletion syndrome)

Some of the symptoms of Monosomy 10pter incude:

Terms associated with Monosomy 10pter:

Terms Similar to Monosomy 10pter:

Source - NIH

Interesting Medical Articles:

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