MeSH Browser

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: 21
Note: mutation in LHCGR
Date of Entry: 2012/11/05
Revision Date: 2013/10/24

Leydig Cell Hypoplasia MeSH Supplementary Concept Data 2024