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Human Disease

primary ovarian insufficiency 15

Term ID
DOID:0080872
Synonyms
Definition
A primary ovarian insufficiency that is characterized by onset of oligomenorrhea in the third decade of life, with small ovaries, reduced number of follicles, and elevated gonadotropic hormones and that has_material_basis_in homozygous mutation in the FANCM gene on chromosome 14q21. https://pubmed.ncbi.nlm.nih.gov/29231814/
References
Ontology
Human Disease   ( DOID:0080872 )
Relationships
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Genes Involved
Zebrafish Models