MeSH Browser

MeSH Supplementary: Ovarian Dysgenesis 2
Unique ID: C564499
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564499
Entry Term(s): Ovarian Dysgenesis, Hypergonadotropic, X-Linked; Ovarian Failure, Hypergonadotropic, Due To Ovarian Dysgenesis; Premature Ovarian Failure 4
Registry Numbers: 0
Heading Mapped to: *Gonadal Dysgenesis; *Genetic Diseases, X-Linked
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Ovarian Dysgenesis 2 MeSH Supplementary Concept Data 2025