spermatogenic failure 22

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Summary

Literature (0)

DOID:0070177 - spermatogenic failure 22

Disease Ontology Definition:A spermatogenic failure that is characterized by autosomal recessive inheritance of spermatocyte maturation arrest resulting in azoospermia that has_material_basis_in mutation in the MEIOB gene on chromosome 16p13.

Synonyms: SPGF22

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: meiob

MIM:

MIM:617706 - SPERMATOGENIC FAILURE 22; SPGF22

MIM:617706 - SPERMATOGENIC FAILURE 22; SPGF22

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), spermatogenic failure (is_a)