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: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II 		disease 0.940 definitive 1.000 0 1 2003 2017
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C1846839
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 31
DEAFNESS, AUTOSOMAL RECESSIVE 31 		disease 0.800 strong 1.000 0 3 1967 2012
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment 		phenotype 0.430 strong 1.000 0 1 2009 2019
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		disease 0.110 None 1.000 0 0 2011 2011
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		disease 0.110 None 1.000 0 0 2007 2007
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		phenotype 0.100 None 1.000 2 2 2017 2018
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C0162701
Disease: Polysomnography
Polysomnography 		phenotype 0.100 None 1.000 1 1 2012 2012
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C0003467
Disease: Anxiety
Anxiety 		disease 0.100 None 0 0
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		phenotype 0.100 None 0 0
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C3279222
Disease: Aplasia/Hypoplasia of the cerebellum
Aplasia/Hypoplasia of the cerebellum 		phenotype 0.100 None 0 0
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss 		phenotype 0.100 None 0 0
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C3665347
Disease: Visual Impairment
Visual Impairment 		phenotype 0.100 None 0 0
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C3665386
Disease: Abnormal vision
Abnormal vision 		phenotype 0.100 None 0 0
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel 		group 0.100 None 0 0
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C4023018
Disease: Subcortical cerebral atrophy
Subcortical cerebral atrophy 		disease 0.100 None 0 0
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C4023551
Disease: Abnormality of dental color
Abnormality of dental color 		phenotype 0.100 None 0 0
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		disease 0.100 None 0 0
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		phenotype 0.100 None 0 0
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C0456909
Disease: Blindness
Blindness 		phenotype 0.100 None 0 0
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C0004134
Disease: Ataxia
Ataxia 		phenotype 0.100 None 0 0
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C0011053
Disease: Deafness
Deafness 		phenotype 0.100 None 0 1
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C0011334
Disease: Dental caries
Dental caries 		disease 0.100 None 0 0
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		disease 0.100 None 0 0
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		whirlin 0.670 0.385 7.7E-05
CUI: C0018524
Disease: Hallucinations
Hallucinations 		disease 0.100 None 0 0