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Leydig Cell Hypoplasia MeSH Supplementary Concept Data 2022


MeSH Supplementary
Leydig Cell Hypoplasia
Unique ID
C562567
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C562567
Entry Term(s)
46,XY Disorder of Sex Development Due To LH Defects
Hypergonadotropic Hypogonadism, Male, Due To LHCGR Defect
LH Resistance Due To LH Receptor Deactivation
Leydig Cell Agenesis
Leydig Cell Hypoplasia with Male Pseudohermaphroditism
Leydig Cell Hypoplasia, Complete
Leydig Cell Hypoplasia, Partial
Leydig Cell Hypoplasia, Type I
Leydig Cell Hypoplasia, Type II
Luteinizing Hormone Resistance, Female
Male Hypergonadotropic Hypogonadism Due To LHCGR Defect
Registry Number
0
Heading Mapped to
Testis / *abnormalities
*Disorder of Sex Development, 46,XY
Frequency
18
Note
mutation in LHCGR
Date of Entry
2012/11/05
Revision Date
2013/10/24
Leydig Cell Hypoplasia Preferred
Luteinizing Hormone Resistance, Female Narrower
Leydig Cell Hypoplasia, Type II Related
46,XY Disorder of Sex Development Due To LH Defects Narrower
Leydig Cell Hypoplasia, Type I Narrower
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