TSPAN12, tetraspanin 12, 23554

N. diseases: 44; N. variants: 15
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: C2750079
Disease: Exudative Vitreoretinopathy 5
Exudative Vitreoretinopathy 5
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 1 12 0.700 limited 1.000 3 12 2010 2012
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 2 4 0.100 None 0 1
CUI: C0004608
Disease: Retinopathy background
Retinopathy background
disease Eye Diseases Disease or Syndrome 4 0.200 None 0
CUI: C0240897
Disease: Retinal exudates
Retinal exudates
phenotype Finding 5 1 0.100 None 0
CUI: C1851402
Disease: Exudative vitreoretinopathy 1
Exudative vitreoretinopathy 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 6 28 0.110 None 1.000 1 1 2010 2010
CUI: C4072980
Disease: Exudative vitreoretinopathy
Exudative vitreoretinopathy
disease Disease or Syndrome 6 2 0.100 None 0
CUI: C0432252
Disease: Osteoporosis with pseudoglioma
Osteoporosis with pseudoglioma
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 12 37 0.010 None 1.000 1 2016 2016
CUI: C0005754
Disease: Congenital blindness
Congenital blindness
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Nervous System Diseases Congenital Abnormality 16 3 0.010 None 1.000 1 2012 2012
Familial Exudative Vitreoretinopathy
disease Congenital Abnormality 19 18 0.200 None 0.864 22 1 2010 2019
CUI: C0344290
Disease: Vitreoretinal degeneration
Vitreoretinal degeneration
disease Disease or Syndrome 20 6 0.100 None 0 1
Persistent Hyperplastic Primary Vitreous
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Congenital Abnormality 33 4 0.010 None 1.000 1 2011 2011
CUI: C0035313
Disease: Retinal Dysplasia
Retinal Dysplasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Congenital Abnormality 34 2 0.010 None 1.000 1 2012 2012
CUI: C0266526
Disease: Norrie disease
Norrie disease
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases Congenital Abnormality 55 28 0.100 None 0 1
CUI: C0339467
Disease: Proliferative retinopathy
Proliferative retinopathy
disease Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome 57 7 0.010 None 1.000 1 2017 2017
CUI: C0005938
Disease: Bone Density
Bone Density
phenotype Clinical Attribute 138 654 0.100 None 1.000 1 1 2018 2018
CUI: C1527390
Disease: Neoplasms, Intracranial
Neoplasms, Intracranial
group Neoplasms; Nervous System Diseases Neoplastic Process 157 4 0.010 None 1.000 1 2019 2019
CUI: C0035344
Disease: Retinopathy of Prematurity
Retinopathy of Prematurity
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 202 16 0.010 None 1.000 1 2019 2019
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder
group Mental Disorders Mental or Behavioral Dysfunction 328 49 0.010 None 1.000 1 2011 2011
CUI: C0015397
Disease: Disorder of eye
Disorder of eye
group Eye Diseases Disease or Syndrome 400 14 0.300 None 0
Meningioma, benign, no ICD-O subtype
disease Neoplasms; Nervous System Diseases Neoplastic Process 404 30 0.010 None 1.000 1 2019 2019
CUI: C0278877
Disease: Adult Meningioma
Adult Meningioma
disease Neoplasms; Nervous System Diseases Neoplastic Process 405 30 0.010 None 1.000 1 2019 2019
CUI: C0025286
Disease: Meningioma
Meningioma
disease Neoplasms; Nervous System Diseases Neoplastic Process 634 43 0.010 None 1.000 1 2019 2019
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases
group Eye Diseases Disease or Syndrome 714 56 0.020 None 1.000 2 2017 2018
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases Disease or Syndrome 852 704 0.010 None 1.000 1 2014 2014
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 972 125 0.010 None 1.000 1 2017 2017