disease has basis in dysfunction of disease has feature ALMS1 Blindness autosomal recessive disease Alstrom syndrome Alss AlstrC6m syndrome (AS) is 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. Alstrom syndrome Alstrom's syndrome Alström syndrome DOID:0050473 GARD:0005787 ICD10:Q87.8 ICD9:759.89 MESH:D056769 MONDO:0008763 MedDRA:10068783 NCIT:C84549 OMIM:203800 Orphanet:64 SCTID:63702009 UMLS:C0268425 alms developmental anomaly of metabolic origin rare diabetes mellitus type 2 inherited renal tubular disease syndrome associated with dilated cardiomyopathy syndromic genetic obesity inborn errors of metabolism syndromic genetic deafness rare renal tubular disease syndromic retinitis pigmentosa nephropathy-associated ciliopathy retinal ciliopathy