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Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism
MeSH Supplementary Concept Data 2024
Details
Concepts
MeSH Supplementary
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism
Unique ID
C565850
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C565850
Entry Term(s)
Boucher-Neuhauser Syndrome
Registry Numbers
0
Heading Mapped to
*Hypogonadism
*Spinocerebellar Ataxias
*Retinal Dystrophies
Frequency
13
Date of Entry
2012/11/05
Revision Date
1955/01/01
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Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism
Preferred
Concept UI
M0566150
Registry Numbers
0
Terms
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism
Preferred Term
Term UI
T831886
Date
10/22/2012
LexicalTag
NON
ThesaurusID
OMIM (2013)
Boucher-Neuhauser Syndrome
Term UI
T807499
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
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