Search Ontology:
Human Disease

primary ovarian insufficiency 19

Term ID
DOID:0112278
Synonyms
  • POF19
  • POI19
  • premature ovarian failure 19
Definition
A primary ovarian insufficiency characterized by irregular menses that cease in the third decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the HSF2BP gene on chromosome 21q22. https://pubmed.ncbi.nlm.nih.gov/32845237/
References
Ontology
Human Disease   ( DOID:0112278 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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