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Three M Syndrome 2 MeSH Supplementary Concept Data 2025


MeSH Supplementary
Three M Syndrome 2
Unique ID
C567862
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567862
Registry Numbers
0
Heading Mapped to
*Dwarfism
*Muscle Hypotonia
Frequency
2
Note
also known as 3M2; associated with mutation in OBSL1
Date of Entry
2012/08/24
Revision Date
2012/08/24
Three M Syndrome 2 Preferred
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