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Disease association ontology term - MONDO:0021573 - oocyte maturation defect 2

Term summary

ID
MONDO:0021573
Name
oocyte maturation defect 2
Ontology or CV name
Disease association
Definition
Any inherited oocyte maturation defect in which the cause of the disease is a mutation in the TUBB8 gene.

Parents

Annotation

Disease association

MONDO:0021573 - oocyte maturation defect 2

References:

Genes: