Simpson-Golabi-Behmel Syndrome, Type 2 MeSH Supplementary Concept Data 2025

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MeSH Supplementary: Simpson-Golabi-Behmel Syndrome, Type 2
Unique ID: C564567
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564567
Registry Numbers: 0
Heading Mapped to: *Abnormalities, Multiple; *Genetic Diseases, X-Linked
Frequency: 6
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Simpson-Golabi-Behmel Syndrome, Type 2 Preferred

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