X-linked spermatogenic failure 2

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Summary

Literature (0)

DOID:0070185 - X-linked spermatogenic failure 2

Disease Ontology Definition:A spermatogenic failure that is characterized by meiotic arrest of spermatocytes and mixed testicular atrophy that has_material_basis_in X-linked inheritance of mutation in the TEX11 gene on chromosome Xq13.

Synonyms: SPGFX2

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

: tex11

MIM:

MIM:309120 - SPERMATOGENIC FAILURE, X-LINKED, 2; SPGFX2

MIM:309120 - SPERMATOGENIC FAILURE, X-LINKED, 2; SPGFX2

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

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

Parent(s): spermatogenic failure (is_a), X-linked recessive disease (is_a)