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Behr syndrome MeSH Supplementary Concept Data 2024


MeSH Supplementary
Behr syndrome
Unique ID
C537669
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C537669
Entry Term(s)
Optic Atrophy, Infantile Hereditary, With Neurologic Abnormalities
Optic atrophy, infantile hereditary, Behr complicated form of
Registry Number
0
Heading Mapped to
*Ataxia
*Intellectual Disability
Optic Atrophy / *congenital
*Spasm
*Hearing Loss
Frequency
16
Note
Optic atrophy in early childhood, associated with ataxia, spasticity, mental retardation, and posterior column sensory loss
Date of Entry
2010/08/25
Revision Date
2013/11/06
Behr syndrome Preferred
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