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Disease association ontology term - MONDO:0014843 - premature ovarian failure 11

Term summary

ID
MONDO:0014843
Name
premature ovarian failure 11
Ontology or CV name
Disease association
Definition
Any primary ovarian failure in which the cause of the disease is a mutation in the ERCC6 gene.

Parents

Annotation

Disease association

MONDO:0014843 - premature ovarian failure 11

References:

Genes: