primary ovarian insufficiency 9

Summary
Definition
A primary ovarian insufficiency that has_material_basis_in compound heterozygous mutation in the HFM1 gene on chromosome 1p22.
Super Class
autosomal recessive disease primary ovarian insufficiency
Disease Ontology
DOID:0080866
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
164045 HFM1 helicase for meiosis 1

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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