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DSH1

Introduction: DSH1

Description of DSH1

DSH1 (medical condition): A very rare syndrome characterized mainly by patches of abnormal skin...more »

See also:

Dyschromatosis symmetrica hereditaria 1:
  »Introduction: Dyschromatosis symmetrica hereditaria 1
  »Symptoms of Dyschromatosis symmetrica hereditaria 1

DSH1: Rare Disease

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

DSH1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that DSH1, or a subtype of DSH1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

DSH1 as a Disease

DSH1: Another name for Dyschromatosis symmetrica hereditaria 1 (or close medical condition association).
  »Introduction: Dyschromatosis symmetrica hereditaria 1
  »Symptoms of Dyschromatosis symmetrica hereditaria 1

DSH1: Related Diseases

DSH1: DSH1 is listed as a type of (or associated with) the following medical conditions in our database:

Causes of DSH1

Some of the causes of DSH1 are included in the list below:

Symptoms of DSH1 (Dyschromatosis symmetrica hereditaria 1)

Some of the symptoms of DSH1 incude:

  • Small localized areas of excessive pigmentation on face
  • Small localized areas of reduced pigmentation on face
  • Abnormal pigmentation on limbs
  • Freckled appearance of face
  • Abnormal pigmentation on penis

DSH1: Related Disease Topics

These medical disease topics may be related to DSH1:

  • skin pigmentation
  • skin freckles
  • abnormal pigmentation on the penia
  • localised facial pigmentation

Terms associated with DSH1:

Terms Similar to DSH1:

Source - NIH

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