An autosomal recessive disease that is characterized by multiorgan dysfunction. The key features are childhood obesity, blindness due to congenital retinal dystrophy, and sensorineural hearing loss with autosomal recessive inheritance and has_material_basis_in mutations in the ALMS1 gene. (Human Disease Ontology, DOID_0050473)
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1 genes involed in the disease alstrom syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
