Assessment
Questionnaire

Have a symptom?
See what questions
a doctor would ask.
 
Dictionary » Cerebellar ataxia, autosomal dominant
 

Cerebellar ataxia, autosomal dominant

Introduction: Cerebellar ataxia, autosomal dominant

Description of Cerebellar ataxia, autosomal dominant

Cerebellar ataxia, autosomal dominant (medical condition): A group of disorder involving slow progressing incoordination...more »

See also:

Spinocerebellar ataxia, autosomal dominant:
  »Introduction: Spinocerebellar ataxia, autosomal dominant
  »Symptoms of Spinocerebellar ataxia, autosomal dominant

Cerebellar ataxia, autosomal dominant: Related Topics

These medical condition or symptom topics may be relevant to medical information for Cerebellar ataxia, autosomal dominant:

Cerebellar ataxia, autosomal dominant: Rare Disease

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Cerebellar ataxia, autosomal dominant as a "rare disease".

Source - Orphanet

Cerebellar ataxia, autosomal dominant as a Disease

Cerebellar ataxia, autosomal dominant: Another name for Spinocerebellar ataxia, autosomal dominant (or close medical condition association).
  »Introduction: Spinocerebellar ataxia, autosomal dominant
  »Symptoms of Spinocerebellar ataxia, autosomal dominant

Cerebellar ataxia, autosomal dominant: Related Diseases

Cerebellar ataxia, autosomal dominant: Cerebellar ataxia, autosomal dominant is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Cerebellar ataxia, autosomal dominant (Spinocerebellar ataxia, autosomal dominant)

Some of the symptoms of Cerebellar ataxia, autosomal dominant incude:

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • Albinism 1
  • Albinism 2
  • Albinism 3
  • Albinism and complete nerve deafness
  • Albinism deafness syndrome
  • Albinism microcephaly digital anomalies
  • Albinism ocular late onset sensorineural deafness
  • Albinism oculocutaneous, Hermansky-Pudlak type
  • Albinism oculocutaneous, Hermansky-Pudlak type 2
  • Albinism partial -- immunodeficiency
  • Albinism platinum form

    Find out more

    Search to find out more about Cerebellar ataxia, autosomal dominant:

      
      
    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