VBCH2

Introduction: VBCH2

Description of VBCH2

VBCH2 (medical condition): A disease which is characterised by early onset osteoporosis.

See also:

Van Buchem disease type 2:
  »Introduction: Van Buchem disease type 2
  »Symptoms of Van Buchem disease type 2

VBCH2: Rare Disease

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

VBCH2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that VBCH2, or a subtype of VBCH2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

VBCH2 as a Disease

VBCH2: Another name for Van Buchem disease type 2 (or close medical condition association).
  »Introduction: Van Buchem disease type 2
  »Symptoms of Van Buchem disease type 2

Symptoms of VBCH2 (Van Buchem disease type 2)

Some of the symptoms of VBCH2 incude:

• Facial nerve palsy
• Perceptive deafness
• Choroideremia
• Facial muscle weakness
• Mental retardation

See full list of 12 symptoms of VBCH2 (Van Buchem disease type 2)

VBCH2: Related Disease Topics

These medical disease topics may be related to VBCH2:

• autosomal dominant disorder

Terms associated with VBCH2:

Terms Similar to VBCH2:

• Van Buchem disease type 2
• Osteosclerosis of the skull and enlarged mandible

Source - NIH

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