Search Ontology:
Human Disease

primary ovarian insufficiency 5

Term ID
DOID:0080862
Synonyms
Definition
A primary ovarian insufficiency that has_material_basis_in heterozygous mutation in the NOBOX gene on chromosome 7q35. https://pubmed.ncbi.nlm.nih.gov/17701902/
References
  • MIM:611548
Ontology
Human Disease   ( DOID:0080862 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations