Source: ALL

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: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C0271829
Disease: Pendred's syndrome
Pendred's syndrome
disease 1.000 definitive 1.000 234 139 1996 2019
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT
disease 0.730 strong 1.000 88 78 1998 2019
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C0018021
Disease: Goiter
Goiter
phenotype 0.700 strong 0.972 36 2 1996 2017
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
Sensorineural Hearing Loss (disorder)
disease 0.700 strong 1.000 35 3 1996 2019
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.700 strong 1.000 29 40 1999 2018
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C0151516
Disease: Thyroid Hypoplasia
Thyroid Hypoplasia
disease 0.410 None 1.000 1 1 2014 2014
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C0749420
Disease: Thyroid Agenesis
Thyroid Agenesis
disease 0.400 None 1.000 1 0 2014 2014
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C1863752
Disease: Enlarged Vestibular Aqueduct
Enlarged Vestibular Aqueduct
phenotype 0.400 strong 1.000 1 0 2002 2002
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C1691779
Disease: Sensory hearing loss
Sensory hearing loss
disease 0.300 None 1.000 3 0 2004 2006
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C0395941
Disease: Mondini defect
Mondini defect
disease 0.300 strong 1.000 1 0 2002 2002
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms
group 0.300 None 1.000 1 0 2007 2007
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
disease 0.300 None 1.000 1 0 2007 2007
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C0001122
Disease: Acidosis
Acidosis
phenotype 0.200 None 1.000 1 0 2003 2003
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
disease 0.170 None 1.000 7 2 2004 2018
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
disease 0.160 None 1.000 6 0 2000 2013
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
Congenital sensorineural hearing loss
disease 0.160 None 1.000 6 0 2002 2011
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C0042571
Disease: Vertigo
Vertigo
phenotype 0.120 None 1.000 2 0 2007 2014
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C0015672
Disease: Fatigue
Fatigue
phenotype 0.120 None 1.000 2 0 2018 2019
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
Sensorineural hearing loss, bilateral
disease 0.110 None 1.000 1 2 2015 2015
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
group 0.110 None 1.000 1 0 2009 2009
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
disease 0.100 None 1.000 31 0 2002 2019
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
Congenital ear anomaly NOS (disorder)
group 0.100 None 1.000 21 0 2001 2020
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C0339789
Disease: Congenital deafness
Congenital deafness
disease 0.100 None 1.000 18 2 1997 2019
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C0004096
Disease: Asthma
Asthma
disease 0.100 None 1.000 11 2 2008 2019
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
solute carrier family 26 member 4 0.507 0.885 9.0E-22
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement
phenotype 0.100 None 1.000 1 1 2018 2018