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Hereditary nephritis

MONDO:0005334

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.

Also known as: hereditary nephritis, familial nephritis, nephritis, familial

151 clinical trials for this condition and its sub-types.

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Sub-types

IgA glomerulonephritis (101) Alport syndrome (17) Immunoglobulin-mediated membranoproliferative glomerulonephritis (9) C3 glomerulonephritis (7) X-linked Alport syndrome (3) Autosomal recessive Alport syndrome (2) Karyomegalic interstitial nephritis (2) Balkan nephropathy (1) Alport syndrome 3b, autosomal recessive (0) Autosomal dominant Alport syndrome (0) Complement factor H deficiency (0) Digenic Alport syndrome (0) Immunodeficiency with factor H anomaly (0)

Broader categories

Disease (618) Inflammatory disease (310) Kidney disorder (202) Hereditary disease (172) Urinary system disorder (62) Nephritis (16) Human disease (14) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by developmental or physiological process (0)
Trials to join now! 63 Not yet recruiting 23 Not yet finished but already full! 23 Completed 37 Terminated 5
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