SLC6A2, solute carrier family 6 member 2, 6530

N. diseases: 238; N. variants: 24
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0865424
Disease: Adult attention deficit hyperactivity disorder
Adult attention deficit hyperactivity disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 20 6 0.010 None 1.000 1 2019 2019
CUI: C0040247
Disease: Tinea
Tinea 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 21 3 0.010 None 1.000 1 2017 2017
CUI: C0272183
Disease: Qualitative abnormality of granulocyte
Qualitative abnormality of granulocyte 		disease Hemic and Lymphatic Diseases Disease or Syndrome 22 0.010 None 1.000 1 2019 2019
CUI: C0948343
Disease: Transfusion-Related Acute Lung Injury
Transfusion-Related Acute Lung Injury 		disease Respiratory Tract Diseases; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 24 3 0.010 None 1.000 1 2012 2012
CUI: C1299624
Disease: Postural Orthostatic Tachycardia Syndrome
Postural Orthostatic Tachycardia Syndrome 		disease Nervous System Diseases Disease or Syndrome 25 1 0.060 None 0.833 6 1 2005 2017
CUI: C0024586
Disease: Malignant Carcinoid Syndrome
Malignant Carcinoid Syndrome 		disease Neoplasms Disease or Syndrome 25 0.010 None 1.000 1 2017 2017
CUI: C1328479
Disease: Pancreatic Endocrine Carcinoma
Pancreatic Endocrine Carcinoma 		disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 29 0.020 None 1.000 2 2017 2019
CUI: C0001818
Disease: Agoraphobia
Agoraphobia 		disease Mental Disorders Mental or Behavioral Dysfunction 29 11 0.010 None 1.000 1 2005 2005
CUI: C0393576
Disease: Chorea Acanthocytosis Syndrome
Chorea Acanthocytosis Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 29 5 0.010 None 1.000 1 2018 2018
CUI: C0349231
Disease: Phobic anxiety disorder
Phobic anxiety disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 31 7 0.010 None 1.000 1 2009 2009
CUI: C0600142
Disease: Hot flushes
Hot flushes 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 32 1 0.010 None 1.000 1 2015 2015
CUI: C0031572
Disease: Phobia, Social
Phobia, Social 		disease Mental Disorders Mental or Behavioral Dysfunction 33 8 0.010 None 1.000 1 2004 2004
CUI: C0559031
Disease: Functional Gastrointestinal Disorders
Functional Gastrointestinal Disorders 		disease Digestive System Diseases Disease or Syndrome 33 0.010 None 1.000 1 2004 2004
CUI: C0011436
Disease: Dentinogenesis Imperfecta
Dentinogenesis Imperfecta 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Congenital Abnormality 35 7 0.010 None 1.000 1 2008 2008
CUI: C2930967
Disease: Gastro-enteropancreatic neuroendocrine tumor
Gastro-enteropancreatic neuroendocrine tumor 		disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 41 4 0.010 None 1.000 1 2015 2015
CUI: C0745130
Disease: Resistant hypertensive disorder
Resistant hypertensive disorder 		disease Cardiovascular Diseases Disease or Syndrome 47 14 0.010 None 1.000 1 1 2018 2018
CUI: C2732618
Disease: Sessile Serrated Adenoma/Polyp
Sessile Serrated Adenoma/Polyp 		disease Neoplastic Process 48 6 0.010 None 1.000 1 2015 2015
CUI: C0025193
Disease: Melancholia
Melancholia 		disease Mental Disorders Mental or Behavioral Dysfunction 51 8 0.010 None 1.000 1 2010 2010
CUI: C0424139
Disease: Anxiety and fear
Anxiety and fear 		disease Mental or Behavioral Dysfunction 51 0.010 None 1.000 1 2018 2018
CUI: C1334011
Disease: High Grade Cervical Intraepithelial Neoplasia
High Grade Cervical Intraepithelial Neoplasia 		disease Neoplasms Neoplastic Process 51 1 0.010 None 1.000 1 2002 2002
CUI: C0564567
Disease: Impulsive character (finding)
Impulsive character (finding) 		phenotype Mental or Behavioral Dysfunction 52 19 0.010 None 1.000 1 1 2004 2004
CUI: C4324563
Disease: Neutrophil extracellular trap formation
Neutrophil extracellular trap formation 		disease Disease or Syndrome 55 0.010 None 1.000 1 2019 2019
CUI: C0025037
Disease: Meckel Diverticulum
Meckel Diverticulum 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 63 0.010 None 1.000 1 2018 2018
CUI: C0424101
Disease: Inattention
Inattention 		phenotype Mental or Behavioral Dysfunction 66 22 0.030 None 1.000 3 3 2004 2018
CUI: C2063866
Disease: Depressive Disorder, Treatment-Resistant
Depressive Disorder, Treatment-Resistant 		disease Mental Disorders Mental or Behavioral Dysfunction 66 19 0.320 None 1.000 2 2012 2015