Source: MGD

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		1.000 Biomarker MGD The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: ultrastructural observations. 6627025

1983
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder) 		0.700 Biomarker MGD The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: ultrastructural observations. 6627025

1983
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.500 Biomarker MGD The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: ultrastructural observations. 6627025

1983
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		0.500 Biomarker MGD The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: ultrastructural observations. 6627025

1983
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		0.500 Biomarker MGD The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: ultrastructural observations. 6627025

1983
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		1.000 Biomarker MGD Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells. 9435277

1998
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder) 		0.700 Biomarker MGD Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells. 9435277

1998
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.500 Biomarker MGD Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells. 9435277

1998
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		0.500 Biomarker MGD Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells. 9435277

1998
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		0.500 Biomarker MGD Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells. 9435277

1998
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		1.000 Biomarker MGD Mutation analysis of the mouse myosin VIIA deafness gene. 9680294

1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder) 		0.700 Biomarker MGD Mutation analysis of the mouse myosin VIIA deafness gene. 9680294

1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.500 Biomarker MGD Mutation analysis of the mouse myosin VIIA deafness gene. 9680294

1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		0.500 Biomarker MGD Mutation analysis of the mouse myosin VIIA deafness gene. 9680294

1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		0.500 Biomarker MGD Mutation analysis of the mouse myosin VIIA deafness gene. 9680294

1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		1.000 Biomarker MGD The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse. 13336002

1956
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder) 		0.700 Biomarker MGD The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse. 13336002

1956
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.500 Biomarker MGD The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse. 13336002

1956
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		0.500 Biomarker MGD The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse. 13336002

1956
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		0.500 Biomarker MGD The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse. 13336002

1956
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		1.000 Biomarker MGD HEARING DEGENERATION IN SHAKER-1 MOUSE. CORRELATION OF PHYSIOLOGICAL OBSERVATIONS WITH BEHAVIORAL RESPONSES AND WITH COCHLEAR ANATOMY. 14198707

1964
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder) 		0.700 Biomarker MGD HEARING DEGENERATION IN SHAKER-1 MOUSE. CORRELATION OF PHYSIOLOGICAL OBSERVATIONS WITH BEHAVIORAL RESPONSES AND WITH COCHLEAR ANATOMY. 14198707

1964
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.500 Biomarker MGD HEARING DEGENERATION IN SHAKER-1 MOUSE. CORRELATION OF PHYSIOLOGICAL OBSERVATIONS WITH BEHAVIORAL RESPONSES AND WITH COCHLEAR ANATOMY. 14198707

1964
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		0.500 Biomarker MGD HEARING DEGENERATION IN SHAKER-1 MOUSE. CORRELATION OF PHYSIOLOGICAL OBSERVATIONS WITH BEHAVIORAL RESPONSES AND WITH COCHLEAR ANATOMY. 14198707

1964
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		0.500 Biomarker MGD HEARING DEGENERATION IN SHAKER-1 MOUSE. CORRELATION OF PHYSIOLOGICAL OBSERVATIONS WITH BEHAVIORAL RESPONSES AND WITH COCHLEAR ANATOMY. 14198707

1964