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Dictionary » Monosomy 18q23
 

Monosomy 18q23

Introduction: Monosomy 18q23

Description of Monosomy 18q23

Monosomy 18q23 (medical condition): A very rare syndrome caused by a deletion of a part...more »

See also:

Chromosome 18, deletion 18q23:
  »Introduction: Chromosome 18, deletion 18q23
  »Symptoms of Chromosome 18, deletion 18q23

Monosomy 18q23: Related Topics

These medical condition or symptom topics may be relevant to medical information for Monosomy 18q23:

Monosomy 18q23: Rare Disease

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

Monosomy 18q23 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Monosomy 18q23, or a subtype of Monosomy 18q23, 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 18q23 as a "rare disease".

Source - Orphanet

Monosomy 18q23 as a Disease

Monosomy 18q23: Another name for Chromosome 18, deletion 18q23 (or close medical condition association).
  »Introduction: Chromosome 18, deletion 18q23
  »Symptoms of Chromosome 18, deletion 18q23

Monosomy 18q23: Related Diseases

Monosomy 18q23: Monosomy 18q23 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Monosomy 18q23 (Chromosome 18, deletion 18q23)

Some of the symptoms of Monosomy 18q23 incude:

Terms associated with Monosomy 18q23:

Terms Similar to Monosomy 18q23:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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