NLM Logo

Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism MeSH Supplementary Concept Data 2024


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
Heading Mapped to
*Hypogonadism
*Spinocerebellar Ataxias
*Retinal Dystrophies
Frequency
13
Date of Entry
2012/11/05
Revision Date
1955/01/01
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism Preferred
page delivered in 0.006s