Optic atrophy and cataract, autosomal dominant [Supplementary Concept]

Date introduced: August 25, 2010

MeSH Unique ID: C537128

Heading Mapped to:

• Cataract/congenital
• Optic Atrophies, Hereditary

Entry Terms:

• Optic atrophy, cataract, and neurologic disorder
• Optic Atrophy 3, Autosomal Dominant
• Opa3, Autosomal Dominant