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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Inherited oocyte maturation defect
Oocyte maturation defect 9
rare
Identifiers
MONDO:0033565
OMIM:619011
Causal genes
TRIP13
Part of
Inherited oocyte maturation defect
Also known as
OOMD9
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