Viljoen Kallis Voges syndrome

Viljoen Kallis Voges syndrome: Related Topics

These medical condition or symptom topics may be relevant to medical information for Viljoen Kallis Voges syndrome:

• Voges

Viljoen Kallis Voges syndrome: Rare Disease

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

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

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Viljoen Kallis Voges syndrome as a "rare disease".

Source - Orphanet

Viljoen Kallis Voges syndrome as a Disease

Viljoen Kallis Voges syndrome (medical condition): See Viljoen Kallis Voges syndrome (disease information).
  »Introduction: Viljoen Kallis Voges syndrome

More information on medical condition: Viljoen Kallis Voges syndrome:

• Information about Viljoen Kallis Voges syndrome
• Basic Summary for Viljoen Kallis Voges syndrome

Terms associated with Viljoen Kallis Voges syndrome:

Terms Similar to Viljoen Kallis Voges syndrome:

• Microcephaly, short stature, brachydactyly type D, flattened occiput, low-set large ears, prominent nose, kyphoscoliosis and mental retardation

Source - NIH

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