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Echinobase
Summary Literature (0)
DOID:0050473 - Alstrom syndrome

Disease Ontology Definition: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:

Echinobase Genes :


OMIM:
MIM:203800 - alstrom syndrome; alms

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), syndrome (is_a)