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: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases Neoplastic Process 311 827 0.010 None 1.000 1 2019 2019
CUI: C0235480
Disease: Paroxysmal atrial fibrillation
Paroxysmal atrial fibrillation
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 226 8 0.010 None 1.000 1 2018 2018
CUI: C0236048
Disease: Polyposis, Gastric
Polyposis, Gastric
disease Digestive System Diseases; Neoplasms Disease or Syndrome 12 4 0.010 None 1.000 1 2014 2014
CUI: C0236663
Disease: Alcohol withdrawal syndrome
Alcohol withdrawal syndrome
disease Chemically-Induced Disorders; Mental Disorders Disease or Syndrome 67 6 0.010 None 1.000 1 2002 2002
CUI: C0236794
Disease: Panic disorder without agoraphobia
Panic disorder without agoraphobia
disease Mental Disorders Mental or Behavioral Dysfunction 3 2 0.010 None < 0.001 1 2 2005 2005
CUI: C0237123
Disease: Alcohol or Other Drugs use
Alcohol or Other Drugs use
disease Mental or Behavioral Dysfunction 108 21 0.010 None 1.000 1 1 2016 2016
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
Gastrointestinal Stromal Tumors
group Digestive System Diseases; Neoplasms Neoplastic Process 538 154 0.010 None 1.000 1 2019 2019
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
disease Neoplasms; Endocrine System Diseases Neoplastic Process 1348 204 0.010 None < 0.001 1 2018 2018
CUI: C0238707
Disease: Impairment of attention
Impairment of attention
disease Mental or Behavioral Dysfunction 5 0.010 None 1.000 1 2016 2016
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders
group Nervous System Diseases Disease or Syndrome 373 95 0.010 None 1.000 1 2 2017 2017
CUI: C0264716
Disease: Chronic heart failure
Chronic heart failure
disease Cardiovascular Diseases Disease or Syndrome 223 11 0.010 None 1.000 1 2018 2018
CUI: C0265008
Disease: Aortocaval fistula
Aortocaval fistula
disease Cardiovascular Diseases Anatomical Abnormality 6 0.010 None 1.000 1 2018 2018
CUI: C0268436
Disease: Pseudohypoaldosteronism, Type I
Pseudohypoaldosteronism, Type I
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 19 0.010 None 1.000 1 2014 2014
Qualitative abnormality of granulocyte
disease Hemic and Lymphatic Diseases Disease or Syndrome 22 0.010 None 1.000 1 2019 2019
CUI: C0278488
Disease: Carcinoma breast stage IV
Carcinoma breast stage IV
disease Neoplastic Process 573 14 0.010 None 1.000 1 2017 2017
CUI: C0278695
Disease: Neuroblastoma recurrent
Neuroblastoma recurrent
disease Neoplasms; Endocrine System Diseases Neoplastic Process 11 2 0.010 None 1.000 1 2019 2019
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 453 235 0.010 None 1.000 1 2006 2006
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: 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: C0232191
Disease: Reflex bradycardia
Reflex bradycardia
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0220664
Disease: BRACHYDACTYLY, TYPE D
BRACHYDACTYLY, TYPE D
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 8 2 0.010 None 1.000 1 2019 2019
CUI: C0029118
Disease: Opportunistic Infections
Opportunistic Infections
group Infections Disease or Syndrome 90 7 0.010 None 1.000 1 1 2003 2003
CUI: C0029434
Disease: Osteogenesis Imperfecta
Osteogenesis Imperfecta
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome; Congenital Abnormality 90 91 0.010 None 1.000 1 1 2003 2003
CUI: C0030297
Disease: Pancreatic Neoplasm
Pancreatic Neoplasm
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 764 20 0.010 None 1.000 1 2017 2017
CUI: C0031572
Disease: Phobia, Social
Phobia, Social
disease Mental Disorders Mental or Behavioral Dysfunction 33 8 0.010 None 1.000 1 2004 2004