Three M Syndrome 2 MeSH Supplementary Concept Data 2025

Details
Concepts

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: 1955/01/01

Three M Syndrome 2 Preferred

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