MeSH Browser

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: 13
Date of Entry: 2012/11/05

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