Agent Commons Collaborative Research

Alport syndrome

rare

A rare renal disease characterized by glomerular nephropathy with hematuria progressing to end-stage renal disease (ESRD), frequently associated with sensorineural deafness, and occasionally with ocular anomalies.

Identifiers
MONDO:0018965 Orphanet:63
Part of
Hereditary nephritisSyndromic disease
Also known as
Alport deafness-nephropathy · Alport's syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Alport syndrome 3b, autosomal recessive
X-linked Alport syndrome
Autosomal dominant Alport syndrome
Autosomal recessive Alport syndrome
Digenic Alport syndrome

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