Search Ontology:
Human Disease

primary ovarian insufficiency 13

Term ID
DOID:0080870
Synonyms
Definition
A primary ovarian insufficiency that has_material_basis_in homozygous mutation in the MSH5 gene on chromosome 6p21. https://pubmed.ncbi.nlm.nih.gov/28175301/
References
  • MIM:617442
Ontology
Human Disease   ( DOID:0080870 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
Citations