SLC2A4, solute carrier family 2 member 4, 6517

N. diseases: 158; N. variants: 7
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: C0342750
Disease: Glycogen storage disease type Id
Glycogen storage disease type Id 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 1 0.010 None 1.000 1 1995 1995
CUI: C2932666
Disease: Gestational Diabetes Insipidus
Gestational Diabetes Insipidus 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C0342311
Disease: Neuroglycopenia
Neuroglycopenia 		disease Nutritional and Metabolic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C1290645
Disease: Dentin bridge
Dentin bridge 		disease Stomatognathic Diseases Disease or Syndrome 5 0.010 None 1.000 1 2020 2020
CUI: C1854181
Disease: FIBROMATOSIS, GINGIVAL, 2
FIBROMATOSIS, GINGIVAL, 2 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Disease or Syndrome 6 0.010 None 1.000 1 2019 2019
CUI: C3827793
Disease: Transient hypothyroxinaemia of prematurity
Transient hypothyroxinaemia of prematurity 		disease Disease or Syndrome 6 0.010 None 1.000 1 2017 2017
CUI: C1135188
Disease: Critical illness myopathy
Critical illness myopathy 		disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 8 0.010 None 1.000 1 2013 2013
CUI: C4054325
Disease: Obesity Related Glomerulopathy
Obesity Related Glomerulopathy 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 16 0.010 None 1.000 1 2018 2018
CUI: C0017924
Disease: Glycogen Storage Disease Type V
Glycogen Storage Disease Type V 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 22 76 0.010 None 1.000 1 2008 2008
CUI: C0231230
Disease: Fatigability
Fatigability 		phenotype Sign or Symptom 29 4 0.010 None 1.000 1 2018 2018
CUI: C0175709
Disease: Centronuclear myopathy
Centronuclear myopathy 		disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 40 13 0.010 None 1.000 1 2017 2017
CUI: C0271790
Disease: Subclinical hypothyroidism
Subclinical hypothyroidism 		disease Endocrine System Diseases Disease or Syndrome 40 10 0.010 None 1.000 1 2019 2019
CUI: C0858600
Disease: Taste sweet
Taste sweet 		phenotype Sign or Symptom 41 3 0.010 None 1.000 1 2019 2019
CUI: C0151798
Disease: Hepatic necrosis
Hepatic necrosis 		phenotype Digestive System Diseases Disease or Syndrome 44 0.010 None 1.000 1 2018 2018
CUI: C0796154
Disease: SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1
SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases; Mental Disorders; Behavior and Behavior Mechanisms; Cardiovascular Diseases Disease or Syndrome 44 12 0.010 None 1.000 1 2019 2019
CUI: C1609524
Disease: ADHF
ADHF 		disease Disease or Syndrome 46 0.010 None 1.000 1 2008 2008
CUI: C0340293
Disease: Anterior myocardial infarction
Anterior myocardial infarction 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 47 3 0.010 None 1.000 1 2017 2017
CUI: C0032969
Disease: Pregnancy in Diabetics
Pregnancy in Diabetics 		phenotype Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 53 1 0.010 None 1.000 1 2017 2017
CUI: C1533172
Disease: Infantile nystagmus syndrome
Infantile nystagmus syndrome 		disease Eye Diseases; Nervous System Diseases Disease or Syndrome 54 8 0.010 None 1.000 1 2013 2013
CUI: C0429468
Disease: Anovulatory (finding)
Anovulatory (finding) 		disease Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Disease or Syndrome 55 8 0.010 None 1.000 1 2019 2019
CUI: C0263630
Disease: Hypertrophic disorder of skin, unspecified
Hypertrophic disorder of skin, unspecified 		group Skin and Connective Tissue Diseases Disease or Syndrome 62 1 0.010 None 1.000 1 2019 2019
CUI: C0920563
Disease: Insulin Sensitivity
Insulin Sensitivity 		phenotype Nutritional and Metabolic Diseases Pathologic Function 62 0.300 None 1.000 1 2002 2002
CUI: C3887551
Disease: Memory dysfunction
Memory dysfunction 		disease Mental Disorders Mental or Behavioral Dysfunction 70 3 0.010 None 1.000 1 2017 2017
CUI: C0004997
Disease: Benign Ovarian Neoplasm
Benign Ovarian Neoplasm 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Neoplastic Process 72 0.010 None 1.000 1 2005 2005
CUI: C3179349
Disease: Gastrointestinal Stromal Sarcoma
Gastrointestinal Stromal Sarcoma 		disease Digestive System Diseases; Neoplasms Neoplastic Process 74 0.010 None 1.000 1 2012 2012