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Albinism, minimal pigment type

Introduction: Albinism, minimal pigment type

Description of Albinism, minimal pigment type

Albinism, minimal pigment type (medical condition): A rare inherited disorder characterized by a total lack of pigmentation...more »

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Albinism, minimal pigment type:
  »Introduction: Albinism, minimal pigment type
  »Symptoms of Albinism, minimal pigment type

Albinism, minimal pigment type: Related Topics

These medical condition or symptom topics may be relevant to medical information for Albinism, minimal pigment type:

Albinism, minimal pigment type: Rare Disease

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

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

Albinism, minimal pigment type as a Disease

Albinism, minimal pigment type (medical condition): See Albinism, minimal pigment type (disease information).
  »Introduction: Albinism, minimal pigment type
  »Symptoms of Albinism, minimal pigment type

Albinism, minimal pigment type: Related Diseases

Albinism, minimal pigment type: Albinism, minimal pigment type is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: Albinism, minimal pigment type:

Terms associated with Albinism, minimal pigment type:

Terms Similar to Albinism, minimal pigment type:

Source - NIH

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