MYO7A, myosin VIIA, 4647

N. diseases: 104; N. variants: 194
Disease: Usher Syndrome, Type II ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II 		0.500 GermlineCausalMutation disease ORPHANET Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2. 24831256 2014
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II 		0.500 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