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Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant MeSH Supplementary Concept Data 2024


MeSH Supplementary
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant
Unique ID
C563497
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C563497
Registry Number
0
Heading Mapped to
*Optic Atrophy
*Peripheral Nervous System Diseases
*Hearing Loss
Frequency
1
Date of Entry
2012/11/05
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant Preferred
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