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spermatogenic failure 4

Disease Summary
Associated Targets (2)
Tbio

2


GARD Rare
Mondo Description Any azoospermia in which the cause of the disease is a mutation in the SYCP3 gene.
Uniprot Description An infertility disorder characterized by azoospermia, a condition of having no sperm present in the ejaculate. Testicular histology shows arrest of spermatogenesis at the pachytene stage of primary spermatocytes.
Disease Ontology Description An azoospermia characterized by autosomal dominant inheritance of nonobstructive azoospermia caused by meiotic abnormalities that has_material_basis_in mutation in the SYCP3 gene on chromosome 12q23.
Mondo Term and Equivalent IDs
MONDO:0010052:  spermatogenic failure 4
GARD:0008530: 
MESH:C536875: