Disease-gene associations mined from literature

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

Linkouts:  OMIM