Neonatal olivopontocerebellar (OPCA) atrophy

Neonatal olivopontocerebellar (OPCA) atrophy: Related Topics

These medical condition or symptom topics may be relevant to medical information for Neonatal olivopontocerebellar (OPCA) atrophy:

• Neonatal
• Neonatal symptoms (13 causes)
• Neonatal disease
• Neonatal disorder
• Olivopontocerebellar
• Olivopontocerebellar syndrome
• OPCA
• Atrophy (351 causes)

Neonatal olivopontocerebellar (OPCA) atrophy: Rare Disease

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

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

Terms associated with Neonatal olivopontocerebellar (OPCA) atrophy:

Terms Similar to Neonatal olivopontocerebellar (OPCA) atrophy:

• Carbohydrate deficient glycoprotein syndrome
• CDGS 1
• Familial olivopontocerebellar atrophy
• Jaeken syndrome

Source - NIH

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Medical dictionaries:

• Medical dictionary,
• Medical Acronymns/Abbreviations

More Medical Dictionary Topics

Kininogen, Low-Molecular-Weight

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