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Dyskeratosis Congenita, Autosomal Dominant
MeSH Supplementary Concept Data 2025
Details
Concepts
MeSH Supplementary
Dyskeratosis Congenita, Autosomal Dominant
Unique ID
C565079
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C565079
Entry Term(s)
Dyskeratosis Congenita, Scoggins Type
Registry Numbers
0
Heading Mapped to
*Dyskeratosis Congenita
Frequency
5
Date of Entry
2012/11/05
Revision Date
1955/01/01
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Dyskeratosis Congenita, Autosomal Dominant
Preferred
Concept UI
M0565379
Registry Numbers
0
Terms
Dyskeratosis Congenita, Autosomal Dominant
Preferred Term
Term UI
T806122
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
Dyskeratosis Congenita, Scoggins Type
Term UI
T806124
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
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