Toggle navigation
Search
Tree View
MeSH on Demand
MeSH 2023
About
Suggestions
Contact Us
Prader-Willi-Like Syndrome Associated With Chromosome 6
MeSH Supplementary Concept Data 2024
Details
Concepts
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
Expand All
Collapse All
Prader-Willi-Like Syndrome Associated With Chromosome 6
Preferred
Concept UI
M0567064
Terms
Prader-Willi-Like Syndrome Associated With Chromosome 6
Preferred Term
Term UI
T809079
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
page delivered in 0.004s