SLC2A10, solute carrier family 2 member 10, 81031

N. diseases: 135; N. variants: 22
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: C4025003
Disease: Aortic tortuosity
Aortic tortuosity 		disease Anatomical Abnormality 1 0.100 None 0
CUI: C0746984
Disease: Obstructive ventilatory defect
Obstructive ventilatory defect 		disease Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C3554587
Disease: Telangiectases of the cheeks
Telangiectases of the cheeks 		phenotype Finding 2 0.100 None 0
CUI: C1836651
Disease: Generalized arterial tortuosity
Generalized arterial tortuosity 		phenotype Finding 4 0.100 None 0
CUI: C4023422
Disease: Long palm
Long palm 		phenotype Finding 5 2 0.100 None 0
CUI: C1336117
Disease: Stage IA Lung Adenocarcinoma AJCC v7
Stage IA Lung Adenocarcinoma AJCC v7 		disease Neoplastic Process 7 3 0.010 None 1.000 1 2017 2017
CUI: C2609059
Disease: Antisynthetase syndrome
Antisynthetase syndrome 		disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 9 0.010 None 1.000 1 2001 2001
CUI: C3887531
Disease: Keratoglobus
Keratoglobus 		disease Anatomical Abnormality 9 0.100 None 0
CUI: C3812396
Disease: Chronic idiopathic pulmonary fibrosis
Chronic idiopathic pulmonary fibrosis 		disease Respiratory Tract Diseases Disease or Syndrome 11 0.010 None 1.000 1 2001 2001
CUI: C1849043
Disease: Soft, doughy skin
Soft, doughy skin 		phenotype Finding 11 4 0.100 None 0
CUI: C0201968
Disease: Cortisol Measurement
Cortisol Measurement 		phenotype Laboratory Procedure 12 16 0.100 None 1.000 1 1 2018 2018
CUI: C4025731
Disease: Abnormal thrombosis
Abnormal thrombosis 		disease Anatomical Abnormality 13 1 0.100 None 0
CUI: C4284120
Disease: Ecstasy related disorders
Ecstasy related disorders 		disease Mental or Behavioral Dysfunction 15 0.010 None 1.000 1 2010 2010
CUI: C2750604
Disease: Median cleft lip and palate
Median cleft lip and palate 		disease Congenital Abnormality 15 0.100 None 0
CUI: C0038449
Disease: Stricture of artery
Stricture of artery 		phenotype Cardiovascular Diseases Pathologic Function 16 0.100 None 0
CUI: C0600228
Disease: Cardiopulmonary Arrest
Cardiopulmonary Arrest 		phenotype Cardiovascular Diseases Pathologic Function 16 0.100 None 0
CUI: C0019288
Disease: Hernia, Femoral
Hernia, Femoral 		disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 18 0.100 None 0
CUI: C2697932
Disease: Loeys-Dietz Syndrome
Loeys-Dietz Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 20 35 0.010 None 1.000 1 2006 2006
CUI: C0002940
Disease: Aneurysm
Aneurysm 		disease Cardiovascular Diseases Pathologic Function 22 36 0.100 None 0 1
CUI: C1442965
Disease: Avascular necrosis of the capital femoral epiphysis
Avascular necrosis of the capital femoral epiphysis 		disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Disease or Syndrome 23 0.100 None 0
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases Disease or Syndrome 29 15 0.010 None 1.000 1 2010 2010
CUI: C4025211
Disease: Abnormal carotid artery morphology
Abnormal carotid artery morphology 		disease Anatomical Abnormality 32 0.100 None 0
CUI: C0023234
Disease: Legg-Calve-Perthes Disease
Legg-Calve-Perthes Disease 		disease Musculoskeletal Diseases Disease or Syndrome 36 9 0.100 None 0
CUI: C0238397
Disease: Pulmonary artery stenosis
Pulmonary artery stenosis 		disease Cardiovascular Diseases Anatomical Abnormality 36 2 0.100 None 0
CUI: C1859726
Disease: ARTERIAL TORTUOSITY SYNDROME
ARTERIAL TORTUOSITY SYNDROME 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 37 23 0.800 strong 0.913 23 20 2003 2020