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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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Spermatogenic failure
Spermatogenic failure 50
Identifiers
MONDO:0030869
OMIM:619145
Causal genes
XRCC2
Part of
Spermatogenic failure
Also known as
spermatogenic failures 50 · SPGF50
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