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Trisomy 22 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Trisomy 22, or a subtype of Trisomy 22,
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 it affects 1 person per 2,000.
They list Trisomy 22 as a "rare disease".
Source - Orphanet
Broader types of Trisomy 22:
Causes of Trisomy 22: see causes of Trisomy 22
Symptoms of Trisomy 22: see symptoms of Trisomy 22
Inheritance of genetic conditions: see details in inheritance of genetic diseases.
Diagnostic testing: see tests for Trisomy 22.
Doctors and Medical Specialists for Trisomy 22: Medical Geneticist
;
see also doctors and medical specialists for Trisomy 22.
Treatments for Trisomy 22:
see treatments for Trisomy 22
Research for Trisomy 22:
see research for Trisomy 22
Organs and body systems related to Trisomy 22 include:
Main name of condition: Trisomy 22
Class of Condition for Trisomy 22: genetic chromosomal, genetic-chromosomal-autosomal
Chromosome 22, trisomy, Duplication 22
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)
Research the causes of these diseases that are similar to, or related to, Trisomy 22:
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