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Dictionary » HSP-TCC
 

HSP-TCC

Introduction: HSP-TCC

Description of HSP-TCC

HSP-TCC (medical condition): A rare genetic disorder characterized by progressive...more »

See also:

Spastic paraplegia 11, autosomal recessive:
  »Introduction: Spastic paraplegia 11, autosomal recessive
  »Symptoms of Spastic paraplegia 11, autosomal recessive

HSP-TCC: Related Topics

These medical condition or symptom topics may be relevant to medical information for HSP-TCC:

HSP-TCC: Rare Disease

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

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

HSP-TCC as a Disease

HSP-TCC: Another name for Spastic paraplegia 11, autosomal recessive (or close medical condition association).
  »Introduction: Spastic paraplegia 11, autosomal recessive
  »Symptoms of Spastic paraplegia 11, autosomal recessive

HSP-TCC: Related Diseases

HSP-TCC: HSP-TCC is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of HSP-TCC (Spastic paraplegia 11, autosomal recessive)

Some of the symptoms of HSP-TCC incude:

  • Progressive lower leg weakness
  • Progressive lower leg spasticity
  • Mental impairment
  • Brain anomaly
  • Slight ataxia

HSP-TCC: Related Disease Topics

These medical disease topics may be related to HSP-TCC:

Terms associated with HSP-TCC:

Terms Similar to HSP-TCC:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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