CLRN1, clarin 1, 7401

N. diseases: 77; N. variants: 26
Disease: Hereditary retinal dystrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.200 Biomarker group MGD Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III. 29044151 2017
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.200 Biomarker group MGD The mechanosensory structure of the hair cell requires clarin-1, a protein encoded by Usher syndrome III causative gene. 22787034 2012
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.200 Biomarker group MGD Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation. 19414487 2009