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Dictionary » Spinocerebellar ataxia 24, (formerly)
 

Spinocerebellar ataxia 24, (formerly)

Introduction: Spinocerebellar ataxia 24, (formerly)

Description of Spinocerebellar ataxia 24, (formerly)

Spinocerebellar ataxia 24, (formerly) (medical condition): A rare neurological disorder caused by a genetic...more »

See also:

Spinocerebellar ataxia, autosomal recessive 4:
  »Introduction: Spinocerebellar ataxia, autosomal recessive 4
  »Symptoms of Spinocerebellar ataxia, autosomal recessive 4

Spinocerebellar ataxia 24, (formerly): Related Topics

These medical condition or symptom topics may be relevant to medical information for Spinocerebellar ataxia 24, (formerly):

Spinocerebellar ataxia 24, (formerly) as a Disease

Spinocerebellar ataxia 24, (formerly): Another name for Spinocerebellar ataxia, autosomal recessive 4 (or close medical condition association).
  »Introduction: Spinocerebellar ataxia, autosomal recessive 4
  »Symptoms of Spinocerebellar ataxia, autosomal recessive 4

Spinocerebellar ataxia 24, (formerly): Related Diseases

Spinocerebellar ataxia 24, (formerly): Spinocerebellar ataxia 24, (formerly) is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Spinocerebellar ataxia 24, (formerly) (Spinocerebellar ataxia, autosomal recessive 4)

Some of the symptoms of Spinocerebellar ataxia 24, (formerly) incude:

Spinocerebellar ataxia 24, (formerly): Related Disease Topics

These medical disease topics may be related to Spinocerebellar ataxia 24, (formerly):

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • Arthrogryposis multiplex congenita, distal, type ii, with craniofacial abnormalities
  • Arthrogryposis multiplex congenita, distal, x-linked
  • Arthrogryposis multiplex congenita, pulmonary hypoplasia, cryptorchidism, and unusual ophthalmological findings
  • Arthrogryposis multiplex congenita, renal dysfunction, and cholestasis
  • Arthrogryposis multiplex congenital
  • Arthrogryposis multiplex congenital Escobar variant form
  • Arthrogryposis multiplex congenital, distal, type ii, with craniofacial abnormalities
  • Arthrogryposis multiplex congenital, distal, type IIa
  • Arthrogryposis renal dysfunction cholestasis
  • Arthrogryposis renal dysfunction cholestasis syndrome
  • Arthrogryposis spinal muscular atrophy
  • Arthrogryposis variant
  • Arthrogryposis with Hyperkeratosis
  • Arthrogryposis with oculomotor limitation and electroretinal abnormalities
  • Arthrogryposis, distal, type 2A

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