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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.
Mondo Term and Equivalent IDs
MONDO:0005334:  hereditary nephritis
EFO:0004128: 
MESH:D009394: 
SCTID:399340005: