VRCP autosomal dominant

Introduction: VRCP autosomal dominant

Description of VRCP autosomal dominant

VRCP autosomal dominant (medical condition): A form of hereditary fundus dystrophy...more »

See also:

Vitreoretinochoroidopathy dominant:
  »Introduction: Vitreoretinochoroidopathy dominant
  »Symptoms of Vitreoretinochoroidopathy dominant

VRCP autosomal dominant: Related Topics

These medical condition or symptom topics may be relevant to medical information for VRCP autosomal dominant:

• Autosomal dominant
• Autosomal dominant disease
• Autosomal dominant disorder
• Autosomal
• Autosomal diseases
• Dominant
• Dominant diseases

VRCP autosomal dominant: Rare Disease

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

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

VRCP autosomal dominant as a Disease

VRCP autosomal dominant: Another name for Vitreoretinochoroidopathy dominant (or close medical condition association).
  »Introduction: Vitreoretinochoroidopathy dominant
  »Symptoms of Vitreoretinochoroidopathy dominant

VRCP autosomal dominant: Related Diseases

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

• Eye and vision conditions
• Head conditions
• Genetic conditions

Symptoms of VRCP autosomal dominant (Vitreoretinochoroidopathy dominant)

Some of the symptoms of VRCP autosomal dominant incude:

• Chorioretinal hypopigmentation
• Hyperpigmentation
• Preretinal punctate white opacities
• Retinal arteriolar narrowing
• Retinal arteriolar occlusion

See full list of 8 symptoms of VRCP autosomal dominant (Vitreoretinochoroidopathy dominant)

VRCP autosomal dominant: Related Disease Topics

These medical disease topics may be related to VRCP autosomal dominant:

• chorioretinal hypopigmentation
• preretinal punctuate white opacities
• retinal arteriolar narrowing
• retinal arteriolar occlusion
• choroidal atrophy
• cataract

Terms associated with VRCP autosomal dominant:

Terms Similar to VRCP autosomal dominant:

• Vitreoretinochoroidopathy dominant
• ADVIRC
• Autosomal dominant Vitreoretinochoroidopathy

Source - NIH

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