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Prader-Willi-Like Syndrome Associated With Chromosome 6 MeSH Supplementary Concept Data 2024


MeSH Supplementary
Prader-Willi-Like Syndrome Associated With Chromosome 6
Unique ID
C566764
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C566764
Heading Mapped to
*Chromosome Deletion
Chromosomes, Human, Pair 6
*Prader-Willi Syndrome
Frequency
1
Date of Entry
2012/11/05
Revision Date
1955/01/01
Prader-Willi-Like Syndrome Associated With Chromosome 6 Preferred
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