Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C4551624
Disease: Idiopathic basal ganglia calcification 1
Idiopathic basal ganglia calcification 1 		0.760 GeneticVariation CLINVAR Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis. 22327515

2012
Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C4551624
Disease: Idiopathic basal ganglia calcification 1
Idiopathic basal ganglia calcification 1 		0.760 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C4324314
Disease: Primary familial brain calcification
Primary familial brain calcification 		0.200 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0029453
Disease: Osteopenia
Osteopenia 		0.110 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0003467
Disease: Anxiety
Anxiety 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0004604
Disease: Back Pain
Back Pain 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0018681
Disease: Headache
Headache 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0020438
Disease: Hypercalciuria
Hypercalciuria 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0030554
Disease: Paresthesia
Paresthesia 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0037763
Disease: Spasm
Spasm 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0042109
Disease: Urticaria
Urticaria 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0079924
Disease: Oligohydramnios
Oligohydramnios 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0085610
Disease: Sinus bradycardia
Sinus bradycardia 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0151480
Disease: Anti-nuclear factor positive
Anti-nuclear factor positive 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0236000
Disease: Jaw pain
Jaw pain 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0401149
Disease: Chronic constipation
Chronic constipation 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0428465
Disease: Serum lipids high (finding)
Serum lipids high (finding) 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0600104
Disease: Obsessive compulsive behavior
Obsessive compulsive behavior 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C0685661
Disease: Congenital anomaly of ischium
Congenital anomaly of ischium 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C1389280
Disease: Basal ganglia calcification
Basal ganglia calcification 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C1854913
Disease: Soft tissue swelling of interphalangeal joints
Soft tissue swelling of interphalangeal joints 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C2673700
Disease: Brisk reflexes
Brisk reflexes 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C4023353
Disease: Abnormality of coordination
Abnormality of coordination 		0.100 CausalMutation CLINVAR

Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C4317146
Disease: Acid reflux
Acid reflux 		0.100 CausalMutation CLINVAR