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spermatogenic failure 14

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any azoospermia in which the cause of the disease is a mutation in the ZMYND15 gene.
Uniprot Description A disorder resulting in the absence (azoospermia) or reduction (oligozoospermia) of sperm in the semen, leading to male infertility.
Disease Ontology Description An azoospermia characterized by autosomal recessive inheritance of a maturation arrest in the spermatid stage of development that has_material_basis_in mutation in the ZMYND15 gene on chromosome 17p13.
Mondo Term and Equivalent IDs
MONDO:0014366:  spermatogenic failure 14
UMLS:C4014454: