SEMA6A, semaphorin 6A, 57556

N. diseases: 211; N. variants: 4
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: C0276839
Disease: Infection by Cytauxzoon
Infection by Cytauxzoon 		phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C2936777
Disease: Nevo syndrome (disorder)
Nevo syndrome (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 3 0.010 None 1.000 1 2005 2005
CUI: C1857025
Disease: Progressive congenital scoliosis
Progressive congenital scoliosis 		disease Musculoskeletal Diseases Congenital Abnormality 4 1 0.010 None 1.000 1 2015 2015
CUI: C0272398
Disease: Dermatopathic lymphadenitis
Dermatopathic lymphadenitis 		disease Hemic and Lymphatic Diseases Disease or Syndrome 6 0.010 None 1.000 1 2006 2006
CUI: C0741975
Disease: carotid disease
carotid disease 		disease Disease or Syndrome 7 5 0.010 None 1.000 1 2017 2017
CUI: C3536593
Disease: Chronic cerebrovascular accident
Chronic cerebrovascular accident 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 7 2 0.010 None 1.000 1 2010 2010
CUI: C4551860
Disease: Ullrich congenital muscular dystrophy
Ullrich congenital muscular dystrophy 		disease Disease or Syndrome 7 0.010 None 1.000 1 2012 2012
CUI: C0017923
Disease: Glycogen Storage Disease Type IV
Glycogen Storage Disease Type IV 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 10 21 0.010 None 1.000 1 2018 2018
CUI: C1302995
Disease: Congenital Fibrosis of the Extraocular Muscles
Congenital Fibrosis of the Extraocular Muscles 		disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 13 4 0.010 None 1.000 1 2019 2019
CUI: C0270724
Disease: Infantile Neuroaxonal Dystrophy
Infantile Neuroaxonal Dystrophy 		disease Nervous System Diseases Disease or Syndrome 17 25 0.010 None 1.000 1 2016 2016
CUI: C0410179
Disease: Ullrich congenital muscular dystrophy 1
Ullrich congenital muscular dystrophy 1 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 17 34 0.010 None 1.000 1 2012 2012
CUI: C0348898
Disease: Irritable bowel syndrome with diarrhea
Irritable bowel syndrome with diarrhea 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 19 0.010 None 1.000 1 2017 2017
CUI: C0398597
Disease: Histiocytic syndrome
Histiocytic syndrome 		disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 21 2 0.010 None 1.000 1 2006 2006
CUI: C1516061
Disease: Astler-Coller B1 Rectal Carcinoma
Astler-Coller B1 Rectal Carcinoma 		disease Neoplastic Process 22 1 0.010 None 1.000 1 2016 2016
CUI: C0039373
Disease: Tay-Sachs Disease
Tay-Sachs Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 26 129 0.010 None 1.000 1 2019 2019
CUI: C0740766
Disease: Acute pneumonia
Acute pneumonia 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 29 0.010 None 1.000 1 2020 2020
CUI: C0019618
Disease: Histiocytosis
Histiocytosis 		disease Hemic and Lymphatic Diseases Neoplastic Process 32 3 0.010 None 1.000 1 2006 2006
CUI: C0240602
Disease: opioid use
opioid use 		disease Mental or Behavioral Dysfunction 39 5 0.010 None 1.000 1 2017 2017
CUI: C0391976
Disease: Pain Disorder
Pain Disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 41 3 0.010 None 1.000 1 2019 2019
CUI: C0265673
Disease: Congenital kyphosis
Congenital kyphosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 54 0.010 None 1.000 1 2015 2015
CUI: C3887709
Disease: Optic Neuropathy
Optic Neuropathy 		disease Eye Diseases; Nervous System Diseases Disease or Syndrome 54 8 0.010 None 1.000 1 2017 2017
CUI: C0024205
Disease: Lymphadenitis
Lymphadenitis 		disease Hemic and Lymphatic Diseases Disease or Syndrome 55 2 0.010 None 1.000 1 2006 2006
CUI: C3887654
Disease: POLYARTERITIS NODOSA, CHILDHOOD-ONSET
POLYARTERITIS NODOSA, CHILDHOOD-ONSET 		disease Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 63 12 0.010 None 1.000 1 2015 2015
CUI: C0410480
Disease: Avascular Necrosis of Femur Head
Avascular Necrosis of Femur Head 		phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Disease or Syndrome 74 20 0.010 None 1.000 1 2019 2019
CUI: C0013720
Disease: Ehlers-Danlos Syndrome
Ehlers-Danlos Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 77 14 0.050 None 1.000 5 2005 2015