THBS2, thrombospondin 2, 7058

N. diseases: 149; N. variants: 13
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: C2676840
Disease: LUMBAR DISC HERNIATION, SUSCEPTIBILITY TO
LUMBAR DISC HERNIATION, SUSCEPTIBILITY TO 		phenotype Finding 1 1 0.100 None 0 1
CUI: C1299240
Disease: Carcinoma of supraglottis
Carcinoma of supraglottis 		disease Neoplastic Process 7 0.010 None 1.000 1 2009 2009
CUI: C0242497
Disease: Intestinal schistosomiasis
Intestinal schistosomiasis 		disease Infections Disease or Syndrome 8 0.010 None 1.000 1 2013 2013
CUI: C2584778
Disease: Thrombotic thrombocytopenic purpura, acquired
Thrombotic thrombocytopenic purpura, acquired 		disease Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 16 1 0.010 None 1.000 1 2011 2011
CUI: C0025945
Disease: Microangiopathy, Diabetic
Microangiopathy, Diabetic 		disease Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome 29 4 0.300 None 1.000 1 2015 2015
CUI: C0860594
Disease: Malignant melanoma, metastatic
Malignant melanoma, metastatic 		disease Neoplasms Neoplastic Process 29 5 0.010 None 1.000 1 2002 2002
CUI: C0750151
Disease: Vaso-Occlusive Crisis
Vaso-Occlusive Crisis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 30 5 0.010 None 1.000 1 2017 2017
CUI: C0751791
Disease: Reflex Epilepsy, Audiogenic
Reflex Epilepsy, Audiogenic 		disease Nervous System Diseases Disease or Syndrome 31 0.010 None 1.000 1 2019 2019
CUI: C3840085
Disease: Disorder of Achilles tendon
Disorder of Achilles tendon 		disease Disease or Syndrome 33 28 0.010 None < 0.001 1 2014 2014
CUI: C0158288
Disease: Spinal stenosis of lumbar region
Spinal stenosis of lumbar region 		disease Musculoskeletal Diseases Disease or Syndrome 34 2 0.010 None 1.000 1 2014 2014
CUI: C1851100
Disease: LAURIN-SANDROW SYNDROME
LAURIN-SANDROW SYNDROME 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 36 0.010 None 1.000 1 2014 2014
CUI: C0796070
Disease: MICROPHTHALMIA, SYNDROMIC 7
MICROPHTHALMIA, SYNDROMIC 7 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases Disease or Syndrome; Congenital Abnormality 46 7 0.010 None 1.000 1 2016 2016
CUI: C0010246
Disease: Coxsackievirus Infections
Coxsackievirus Infections 		group Infections Disease or Syndrome 48 1 0.010 None 1.000 1 2012 2012
CUI: C0699753
Disease: Cancer Relapse
Cancer Relapse 		disease Neoplastic Process 48 0.010 None 1.000 1 2016 2016
CUI: C0221775
Disease: Lumbar disc disease
Lumbar disc disease 		disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Disease or Syndrome 49 30 0.300 None 0
CUI: C3160815
Disease: Intraductal papillary mucinous neoplasm
Intraductal papillary mucinous neoplasm 		disease Neoplastic Process 50 2 0.010 None 1.000 1 2019 2019
CUI: C0281899
Disease: Prolapsed lumbar disc
Prolapsed lumbar disc 		disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Acquired Abnormality 75 33 0.010 None 1.000 1 1 2008 2008
CUI: C1334177
Disease: Infiltrating Cervical Carcinoma
Infiltrating Cervical Carcinoma 		disease Neoplastic Process 76 13 0.010 None 1.000 1 2001 2001
CUI: C0151936
Disease: Disorder of tendon
Disorder of tendon 		group Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 79 14 0.010 None < 0.001 1 1 2014 2014
CUI: C1568272
Disease: Tendinopathy
Tendinopathy 		disease Musculoskeletal Diseases; Wounds and Injuries Disease or Syndrome 80 16 0.010 None < 0.001 1 1 2014 2014
CUI: C1867743
Disease: Premature coronary artery atherosclerosis
Premature coronary artery atherosclerosis 		phenotype Cardiovascular Diseases Disease or Syndrome 87 43 0.010 None 1.000 1 1 2002 2002
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		phenotype Finding 90 119 0.100 None 1.000 1 1 2019 2019
CUI: C1956089
Disease: Osteophyte
Osteophyte 		disease Musculoskeletal Diseases Disease or Syndrome 91 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 1999 1999
CUI: C0266449
Disease: Congenital anomaly of brain
Congenital anomaly of brain 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Nervous System Diseases Congenital Abnormality 103 7 0.010 None 1.000 1 2015 2015