MYO7A, myosin VIIA, 4647

N. diseases: 104; N. variants: 194
Disease: Usher Syndrome, Type III ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1568248
Disease: Usher Syndrome, Type III
Usher Syndrome, Type III 		0.310 Biomarker disease CTD_human Identification of a rat model for usher syndrome type 1B by N-ethyl-N-nitrosourea mutagenesis-driven forward genetics. 15965244 2005
CUI: C1568248
Disease: Usher Syndrome, Type III
Usher Syndrome, Type III 		0.310 Biomarker disease BEFREE The gene encoding human myosin VIIA is responsible for Usher syndrome type III (USH1B), a disease which associates profound congenital sensorineural deafness, vestibular dysfunction, and retinitis pigmentosa. 8622919 1996