Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0006625
Disease: Cachexia
Cachexia 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0008489
Disease: Chorea
Chorea 		0.100 GeneticVariation CLINVAR

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0013132
Disease: Drooling
Drooling 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0013421
Disease: Dystonia
Dystonia 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0014877
Disease: Esotropia
Esotropia 		0.100 GeneticVariation CLINVAR

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0015732
Disease: Fecal Incontinence
Fecal Incontinence 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0016506
Disease: Foot Deformities
Foot Deformities 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		0.100 GeneticVariation CLINVAR

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0025362
Disease: Mental Retardation
Mental Retardation 		0.100 CausalMutation CLINVAR

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0026884
Disease: Mutism
Mutism 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0028738
Disease: Nystagmus
Nystagmus 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		0.100 GeneticVariation CLINVAR

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0037317
Disease: Sleep disturbances
Sleep disturbances 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0037317
Disease: Sleep disturbances
Sleep disturbances 		0.100 GeneticVariation CLINVAR

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0038379
Disease: Strabismus
Strabismus 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0042024
Disease: Urinary Incontinence
Urinary Incontinence 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0152421
Disease: Macrotia
Macrotia 		0.100 Biomarker HPO

Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0234533
Disease: Generalized seizures
Generalized seizures 		0.100 Biomarker HPO