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Hypogonadotropic hypogonadism and anosmia, autosomal dominant MeSH Supplementary Concept Data 2024


MeSH Supplementary
Hypogonadotropic hypogonadism and anosmia, autosomal dominant
Unique ID
C538534
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C538534
Heading Mapped to
*Kallmann Syndrome
Frequency
1
Date of Entry
2010/08/25
Revision Date
1955/01/01
Hypogonadotropic hypogonadism and anosmia, autosomal dominant Preferred
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