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spermatogenic failure 9
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any azoospermia in which the cause of the disease is a mutation in the DPY19L2 gene.
Uniprot Description An infertility disorder caused by spermatogenesis defects. The most prominent feature is the malformation of the acrosome, which can be totally absent in most severe cases. Additional features are an abnormal nuclear shape and abnormal arrangement of the mitochondria of the spermatozoon.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0070175
OMIM:613958
UMLS:C3151407
MONDO:0013505
High level summary of knowledge for a disease, including descriptions and datasource references.