PomBase home

Disease association ontology term - MONDO:0005334 - hereditary nephritis

Term summary

ID
MONDO:0005334
Name
hereditary nephritis
Ontology or CV name
Disease association
Definition
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.

Parents

Annotation

Disease association

MONDO:0018965 - Alport syndrome

References:

Genes:

MONDO:0013898 - karyomegalic interstitial nephritis

References:

Genes: