Search Ontology:
Human Disease

primary ovarian insufficiency 6

Term ID
DOID:0080863
Synonyms
Definition
A primary ovarian insufficiency that has_material_basis_in heterozygous or homozygous mutation in the FIGLA gene on chromosome 2p13. https://pubmed.ncbi.nlm.nih.gov/18499083/
References
Ontology
Human Disease   ( DOID:0080863 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models