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hereditary nephritis
Disease Summary
Associated Targets (545)
Tbio
373
Tchem
104
Tdark
39
Tclin
29
Mondo Description A group of inherited conditions characterized initially by hematuria and slowly progressing to renal insufficiency. The most common form is the Alport syndrome (hereditary nephritis with hearing loss) which is caused by mutations in genes for type IV collagen and defective glomerular basement membrane.
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.
EFO:0004128
MESH:D009394
SCTID:399340005
MONDO:0005334
High level summary of knowledge for a disease, including descriptions and datasource references.