TSPAN33, tetraspanin 33, 340348

N. diseases: 69; N. variants: 0
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: C0265098
Disease: Basilar artery occlusion
Basilar artery occlusion
disease Nervous System Diseases; Cardiovascular Diseases Anatomical Abnormality 4 0.010 None 1.000 1 2017 2017
CUI: C3854333
Disease: Narrowing
Narrowing
disease Anatomical Abnormality 8 0.010 None 1.000 1 2018 2018
CUI: C0751378
Disease: Neurologic Signs
Neurologic Signs
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 13 1 0.010 None 1.000 1 2017 2017
CUI: C0151950
Disease: Deep thrombophlebitis
Deep thrombophlebitis
disease Cardiovascular Diseases Disease or Syndrome 16 0.010 None 1.000 1 2019 2019
CUI: C0037198
Disease: Sinus Thrombosis, Intracranial
Sinus Thrombosis, Intracranial
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 17 5 0.020 None 1.000 2 2018 2019
CUI: C0856120
Disease: Multiple sclerosis relapse
Multiple sclerosis relapse
disease Disease or Syndrome 19 0.010 None < 0.001 1 2019 2019
CUI: C2745948
Disease: Hyalinosis, Systemic
Hyalinosis, Systemic
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 20 30 0.010 None 1.000 1 2019 2019
CUI: C2215101
Disease: Acute cerebral ischemia
Acute cerebral ischemia
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 47 2 0.010 None 1.000 1 2018 2018
CUI: C1285498
Disease: Vegetation
Vegetation
disease Anatomical Abnormality 67 0.010 None < 0.001 1 2019 2019
CUI: C0265101
Disease: Carotid artery occlusion
Carotid artery occlusion
phenotype Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 74 1 0.010 None 1.000 1 2019 2019
CUI: C0338480
Disease: Common Migraine
Common Migraine
disease Nervous System Diseases Disease or Syndrome 77 62 0.010 None 1.000 1 2018 2018
CUI: C0154723
Disease: Migraine with Aura
Migraine with Aura
disease Nervous System Diseases Disease or Syndrome 87 56 0.010 None 1.000 1 2018 2018
CUI: C0162830
Disease: Dermatitis, Phototoxic
Dermatitis, Phototoxic
disease Skin and Connective Tissue Diseases Disease or Syndrome 89 0.010 None 1.000 1 2019 2019
CUI: C1510885
Disease: Angiogenic Switch
Angiogenic Switch
disease Neoplastic Process 96 3 0.010 None 1.000 1 2018 2018
CUI: C0917805
Disease: Transient Cerebral Ischemia
Transient Cerebral Ischemia
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 98 9 0.010 None 1.000 1 2017 2017
CUI: C0432283
Disease: Osteoglophonic dwarfism
Osteoglophonic dwarfism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 100 4 0.010 None 1.000 1 2019 2019
CUI: C0751955
Disease: Brain Infarction
Brain Infarction
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 114 11 0.020 None 1.000 2 2013 2018
CUI: C0279070
Disease: Adult Oligodendroglioma
Adult Oligodendroglioma
disease Neoplasms Neoplastic Process 154 19 0.010 None 1.000 1 2015 2015
CUI: C0280475
Disease: Childhood Oligodendroglioma
Childhood Oligodendroglioma
disease Neoplasms Neoplastic Process 154 19 0.010 None 1.000 1 2015 2015
CUI: C0751956
Disease: Acute Cerebrovascular Accidents
Acute Cerebrovascular Accidents
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 155 2 0.100 None 1.000 12 2005 2019
CUI: C0027873
Disease: Neuromyelitis Optica
Neuromyelitis Optica
disease Eye Diseases; Immune System Diseases; Nervous System Diseases Disease or Syndrome 171 45 0.010 None 1.000 1 2014 2014
CUI: C0221505
Disease: Lesion of brain
Lesion of brain
group Disease or Syndrome 188 9 0.010 None 1.000 1 2018 2018
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis
disease Cardiovascular Diseases Disease or Syndrome 230 93 0.010 None 1.000 1 2019 2019
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
Androgen-Insensitivity Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 247 176 0.030 None 1.000 3 2018 2020
CUI: C1510472
Disease: Drug Dependence
Drug Dependence
group Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 248 31 0.010 None 1.000 1 2019 2019