FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term X-linked spermatogenic failure 9 ID (Ontology) DOID:0061177 (Human Disease)
Definition A spermatogenic failure that is characterized by male infertility due to nonobstructive azoospermia resulting from maturation arrest that has_material_basis_in hemizygous mutation in the RBBP7 gene on chromosome Xp22.
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Human Disease Models (FBhh)  DOID       1
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 Genes Human Disease Models
 X-linked spermatogenic failure 9       1      1
 for disease ribbon | X-linked spermatogenic failure 9       1       --
 model of | X-linked spermatogenic failure 9       1       --
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X-linked monogenic disease
 |__X-linked recessive disease__
male infertility                |
 |__spermatogenic failure_______|
                                X-linked spermatogenic failure 9  2 rec.
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Is a X-linked recessive disease
spermatogenic failure
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MIM:301137