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Summary Literature (0)
OMIM:415000 - SPERMATOGENIC FAILURE, Y-LINKED, 2; SPGFY2


Xenbase Genes: ddx3y

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010767 - spermatogenic failure, Y-linked, 2
MONDO:0015607 - partial chromosome Y deletion

Disease Ontology (DO):
DOID:0070187 - Y-linked spermatogenic failure 2
DOID:14227 - azoospermia