primary ovarian insufficiency 3

Summary
Definition
A primary ovarian insufficiency that has_material_basis_in heterozygous mutation in the FOXL2 gene on chromosome 3q22.
Super Class
autosomal dominant disease primary ovarian insufficiency
Disease Ontology
DOID:0080860
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
668 FOXL2 forkhead box L2

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024