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Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency
MeSH Supplementary Concept Data 2023
Details
Concepts
MeSH Supplementary
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency
Unique ID
C567709
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567709
Entry Term(s)
Myopathy, Congenital, Due To Integrin Alpha-7 Deficiency
Registry Number
0
Heading Mapped to
*Muscular Dystrophies
Frequency
0
Note
mutations in
ITGA7
Date of Entry
2012/11/05
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Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency
Preferred
Concept UI
M0568009
Registry Number
0
Terms
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency
Preferred Term
Term UI
T810925
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
Myopathy, Congenital, Due To Integrin Alpha-7 Deficiency
Term UI
T810926
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
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