MeSH Browser

MeSH Supplementary: Mousa Al din Al Nassar syndrome
Unique ID: C536989
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536989
Entry Term(s): Bedouin spastic ataxia syndrome
Registry Numbers: 0
Heading Mapped to: *Abnormalities, Multiple; *Cataract; *Corneal Dystrophies, Hereditary; *Myopia; *Spinocerebellar Degenerations
Frequency: 0
Note: Spinocerebellar Degeneration With Macular Corneal Dystrophy, Congenital Cataracts, And Myopia
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Mousa Al din Al Nassar syndrome MeSH Supplementary Concept Data 2025