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MVP

MVP: Rare Disease

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

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

MVP as a Disease

MVP: Another name for Mitral valve prolapse, familial, X-linked (or close medical condition association).
  »Introduction: Mitral valve prolapse, familial, X-linked
  »Symptoms of Mitral valve prolapse, familial, X-linked

MVP: Related Diseases

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

Symptoms of MVP (Mitral valve prolapse, familial, X-linked)

Some of the symptoms of MVP incude:

MVP: Related Disease Topics

These medical disease topics may be related to MVP:

Terms associated with MVP:

Terms Similar to MVP:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • Dominant negative mutation
  • Dominant optic atrophy
  • Dominant optic atrophy, deafness, ptosis, ophthalmoplegia, dystaxia, and myopathy
  • Dominant preaxial brachydactyly with hallux varus and thumb abduction
  • Dominant R wave in V1
  • Dominant radial drusen
  • Dominant trait
  • Dominant zonular cataract
  • Dominantly inherited blepharoptosis, high myopia, and ectopia lentis
  • Dominantly inherited bone dysplasia with severe eye involvement
  • Dominantly inherited craniodiaphyseal dysplasia
  • Dominantly inherited keratitis
  • Dominantly inherited LÚvi disease
  • Dominantly inherited ptosis, strabismus and ectopic pupils

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