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Dictionary » Monosomy 1p32
 

Monosomy 1p32

Introduction: Monosomy 1p32

Description of Monosomy 1p32

Monosomy 1p32 (medical condition): A rare chromosomal disorder where deletion of a portion of...more »

See also:

Chromosome 1, monosomy 1p32:
  »Introduction: Chromosome 1, monosomy 1p32
  »Symptoms of Chromosome 1, monosomy 1p32

Monosomy 1p32: Related Topics

These medical condition or symptom topics may be relevant to medical information for Monosomy 1p32:

Monosomy 1p32: Rare Disease

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

Monosomy 1p32 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Monosomy 1p32, or a subtype of Monosomy 1p32, 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 1p32 as a "rare disease".

Source - Orphanet

Monosomy 1p32 as a Disease

Monosomy 1p32: Another name for Chromosome 1, monosomy 1p32 (or close medical condition association).
  »Introduction: Chromosome 1, monosomy 1p32
  »Symptoms of Chromosome 1, monosomy 1p32

Monosomy 1p32: Related Diseases

Monosomy 1p32: Monosomy 1p32 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Monosomy 1p32 (Chromosome 1, monosomy 1p32)

Some of the symptoms of Monosomy 1p32 incude:

Monosomy 1p32: Related Disease Topics

These medical disease topics may be related to Monosomy 1p32:

Terms associated with Monosomy 1p32:

Terms Similar to Monosomy 1p32:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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