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spermatogenic failure, X-linked, 2

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any azoospermia in which the cause of the disease is a mutation in the TEX11 gene.
Uniprot Description An infertility disorder caused by spermatogenesis defects. It is characterized by mixed testicular atrophy and azoospermia with meiotic arrest.
Disease Ontology Description An azoospermia 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.
Mondo Term and Equivalent IDs
MONDO:0010647:  spermatogenic failure, X-linked, 2
UMLS:C1839841: