" /> Spermatogenic failure, y-linked, 2 - CISMeF





Preferred Label : Spermatogenic failure, y-linked, 2;

Symbol : SPGFY2;

CISMeF acronym : SPGFY2;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Spermatogenic arrest, y-linked; Oligozoospermia, nonobstructive, y-linked; Oligospermia, nonobstructive, y-linked; Azoospermia, nonobstructive, y-linked; Spermatogenic failure, nonobstructive, y-linked;

Included titles and symbols : Azoospermia factor regions; Azf regions;

Description : About 2 to 3% of human males are infertile because of defects in sperm function, primarily due to oligozoospermia (defined as less than 10-15 million sperm per mL of semen) or azoospermia (Hull et al., 1985). - Heterogeneity of Spermatogenic Failure For a discussion of Y-linked spermatogenic failure due to Sertoli cell-only syndrome, see 400042. For a discussion of phenotypic and genetic heterogeneity of spermatogenic failure, see SPGF1 (258150).;

Inheritance : Y-linked (Yq11.23);

Prefixed ID : #415000;

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03/05/2025


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