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Dictionary » Westerhof Beemer Cormane syndrome
 

Westerhof Beemer Cormane syndrome

Introduction: Westerhof Beemer Cormane syndrome

Description of Westerhof Beemer Cormane syndrome

Westerhof Beemer Cormane syndrome (medical condition): A rare inherited genetic disorder involving small flat areas increased and...more »

See also:

Macules, hereditary, congenital hypopigmented and hyperpigmented:
  »Introduction: Macules, hereditary, congenital hypopigmented and hyperpigmented
  »Symptoms of Macules, hereditary, congenital hypopigmented and hyperpigmented

Westerhof Beemer Cormane syndrome: Rare Disease

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

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

Westerhof Beemer Cormane syndrome as a Disease

Westerhof Beemer Cormane syndrome: Another name for Macules, hereditary, congenital hypopigmented and hyperpigmented (or close medical condition association).
  »Introduction: Macules, hereditary, congenital hypopigmented and hyperpigmented
  »Symptoms of Macules, hereditary, congenital hypopigmented and hyperpigmented

Westerhof Beemer Cormane syndrome: Related Diseases

Westerhof Beemer Cormane syndrome: Westerhof Beemer Cormane syndrome is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Westerhof Beemer Cormane syndrome (Macules, hereditary, congenital hypopigmented and hyperpigmented)

Some of the symptoms of Westerhof Beemer Cormane syndrome incude:

Terms associated with Westerhof Beemer Cormane syndrome:

Terms Similar to Westerhof Beemer Cormane syndrome:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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