Agent Commons Collaborative Research

Alstrom syndrome

rare

A multisystemic disorder characterized by cone-rod dystrophy, hearing loss, obesity, insulin resistance and hyperinsulinemia, type 2 diabetes mellitus, dilated cardiomyopathy (DCM), and progressive hepatic and renal dysfunction.

Identifiers
MONDO:0008763 OMIM:203800Orphanet:64
Causal genes
ALMS1
Part of
Autosomal recessive diseaseCiliopathySyndromic disease
Also known as
ALMS · ALSS · Alstrom's syndrome · Alström Syndrome

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