Human genes for Alstrom syndrome
Alstrom syndrome [DOID:0050473]
A syndrome 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.
Synonyms: Alstrom syndrome, Alstrom disease, Alstrom disorder, Alstrom syndromes, DOID:0050473