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spermatogenic failure 17

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any azoospermia in which the cause of the disease is a mutation in the PLCZ1 gene.
Uniprot Description An autosomal recessive infertility disorder due to failure of oocyte activation and fertilization by sperm that otherwise exhibits normal morphology.
Disease Ontology Description A male infertility characterized by autosomal recessive inheritance of oocyte activation failure following intracytoplasmic sperm injection that has_material_basis_in mutation in the PLCZ1 gene on chromosome 12p12.
Mondo Term and Equivalent IDs
MONDO:0014970:  spermatogenic failure 17
UMLS:C4310666: