Source: INFERRED

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C1847089
Disease: USHER SYNDROME, TYPE IG
USHER SYNDROME, TYPE IG 		disease 0.920 None 1.000 0 8 1992 2017
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment 		phenotype 0.620 strong 1.000 0 3 2014 2019
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		disease 0.450 definitive 1.000 3 3 2002 2016
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		disease 0.160 None 1.000 0 0 1998 2018
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		disease 0.110 None 1.000 0 0 2009 2009
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss 		phenotype 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C3279222
Disease: Aplasia/Hypoplasia of the cerebellum
Aplasia/Hypoplasia of the cerebellum 		phenotype 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C0003467
Disease: Anxiety
Anxiety 		disease 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C1865866
Disease: Congenital sensorineural hearing loss
Congenital sensorineural hearing loss 		disease 0.100 None 0 1
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C3665347
Disease: Visual Impairment
Visual Impairment 		phenotype 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C3665386
Disease: Abnormal vision
Abnormal vision 		phenotype 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		group 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C4021651
Disease: Hypoplasia of the nasal bone
Hypoplasia of the nasal bone 		phenotype 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel 		group 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C4023018
Disease: Subcortical cerebral atrophy
Subcortical cerebral atrophy 		disease 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology 		disease 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C4072872
Disease: obsolete Rod-cone dystrophy
obsolete Rod-cone dystrophy 		disease 0.100 None 0 1
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		disease 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		phenotype 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C1848606
Disease: Vestibular hypofunction
Vestibular hypofunction 		phenotype 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C0004134
Disease: Ataxia
Ataxia 		phenotype 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C0011053
Disease: Deafness
Deafness 		phenotype 0.100 None 0 2
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C0018524
Disease: Hallucinations
Hallucinations 		disease 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		disease 0.100 None 0 0
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C0018979
Disease: Hemianopsia
Hemianopsia 		disease 0.100 None 0 0