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male infertility with azoospermia or oligozoospermia due to single gene mutation
Disease Summary
Associated Targets (13)
Tbio
10
Tclin
1
Tchem
1
Tdark
1
Mondo Description Male infertility with azoospermia or oligospermia due to single gene mutation is a rare, genetic male infertility due to sperm disorder characterized by the absence of a measurable amount of spermatozoa in the ejaculate (azoospermia), or a number of sperm in the ejaculate inferior to 15 million/mL (oligozoospermia), resulting from a mutation in a single gene known to cause azoo- or oligo-spermia. Sperm morphology may be normal.
Mondo Term and Equivalent IDs
MONDO:0018393: male infertility with azoospermia or oligozoospermia due to single gene mutation
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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.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
Orphanet:399805
UMLS:CN225947
MONDO:0018393
High level summary of knowledge for a disease, including descriptions and datasource references.