Assessment
Questionnaire

Have a symptom?
See what questions
a doctor would ask.
 
Dictionary » Hromosome 13 trisomy syndrome
 

Hromosome 13 trisomy syndrome

Introduction: Hromosome 13 trisomy syndrome

Description of Hromosome 13 trisomy syndrome

Hromosome 13 trisomy syndrome (medical condition): A rare and very severe chromosome disorder leading to mental retardation and physical defects. It is so ...more

Hromosome 13 trisomy syndrome: See also:

Patau syndrome:
  »Introduction: Patau syndrome
  »Symptoms of Patau syndrome

Hromosome 13 trisomy syndrome: Related Topics

These medical condition or symptom topics may be relevant to medical information for Hromosome 13 trisomy syndrome:

Hromosome 13 trisomy syndrome: Rare Disease

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

Hromosome 13 trisomy syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Hromosome 13 trisomy syndrome, or a subtype of Hromosome 13 trisomy syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Hromosome 13 trisomy syndrome as a Disease

Hromosome 13 trisomy syndrome: Another name for Patau syndrome (or close medical condition association).
  »Introduction: Patau syndrome
  »Symptoms of Patau syndrome

Hromosome 13 trisomy syndrome: Related Diseases

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

Symptoms of Hromosome 13 trisomy syndrome (Patau syndrome)

Some of the symptoms of Hromosome 13 trisomy syndrome incude:

Hromosome 13 trisomy syndrome: Related Disease Topics

These medical disease topics may be related to Hromosome 13 trisomy syndrome:

Terms associated with Hromosome 13 trisomy syndrome:

Terms Similar to Hromosome 13 trisomy syndrome:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • Hyperthyroid Grave's disease
  • Hyperthyroid heart
  • Hyperthyroidism
  • Hyperthyroidism due to mutations in TSH receptor
  • Hyperthyroidism, familial, due to mutations in TSH receptor
  • Hyperthyroxinemia
  • Hyperthyroxinemia, eumetabolic, due to T4 plasma membrane transport
  • Hyperthyroxinemia, eumetabolic, due to T4 plasma membrane transport defect
  • Hyperthyroxinemia, Familial Dysalbuminemic
  • Hypertonia

    Find out more

    Search to find out more about Hromosome 13 trisomy syndrome:

      
      
    powered by
    Google
  •  

    By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.

    Home | Symptoms | Diseases | Diagnosis | Videos | Tools | Forum | About Us | Terms of Use | Privacy Policy | Site Map | Advertise