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Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism MeSH Supplementary Concept Data 2022


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 Number
0
Heading Mapped to
*Hypogonadism
*Spinocerebellar Ataxias
*Retinal Dystrophies
Frequency
12
Date of Entry
2012/11/05
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism Preferred
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