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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease wolfram syndrome
Comorbidity C0011849|diabetes mellitus
Sentences 3
PubMedID- 26426397 Although the connection between loss of function mutations of the wfs1 gene and didmoad-syndrome including diabetes mellitus underpins the significance of wolframin in the pathogenesis, exact role of wfs1 polymorphic variants in the development of type 1 and type 2 diabetes has not been discovered yet.
PubMedID- 22737327 One should consider wolfram syndrome in patients with juvenile onset diabetes mellitus and hearing loss.
PubMedID- 23257691 Association of rs734312 and rs10010131 polymorphisms in wfs1 gene with type 2 diabetes mellitus: a meta-analysis.

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