CLDN5, claudin 5, 7122

N. diseases: 104; N. variants: 2
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: C0349554
Disease: Vaginal intraepithelial neoplasia grade 1
Vaginal intraepithelial neoplasia grade 1 		disease Neoplastic Process 2 0.010 None 1.000 1 2012 2012
CUI: C0349555
Disease: Vaginal intraepithelial neoplasia grade 2
Vaginal intraepithelial neoplasia grade 2 		disease Neoplastic Process 4 0.010 None 1.000 1 2012 2012
CUI: C0278650
Disease: Childhood Supratentorial Ependymoma
Childhood Supratentorial Ependymoma 		disease Neoplasms Neoplastic Process 12 0.010 None 1.000 1 2017 2017
CUI: C0270933
Disease: Inflammatory neuropathy
Inflammatory neuropathy 		disease Nervous System Diseases Disease or Syndrome 19 1 0.010 None 1.000 1 2004 2004
CUI: C0035228
Disease: Respiratory Hypersensitivity
Respiratory Hypersensitivity 		phenotype Respiratory Tract Diseases; Immune System Diseases Pathologic Function 23 0.300 None 1.000 1 2019 2019
CUI: C0400822
Disease: Colitis, Lymphocytic
Colitis, Lymphocytic 		disease Digestive System Diseases Disease or Syndrome 25 0.010 None 1.000 1 2017 2017
CUI: C1306557
Disease: Chronic venous insufficiency
Chronic venous insufficiency 		disease Cardiovascular Diseases Disease or Syndrome 25 3 0.010 None 1.000 1 2006 2006
CUI: C0400821
Disease: Colitis, Microscopic
Colitis, Microscopic 		disease Digestive System Diseases Disease or Syndrome 30 3 0.010 None 1.000 1 2017 2017
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 31 2 0.010 None 1.000 1 2018 2018
CUI: C0037036
Disease: Sialorrhea
Sialorrhea 		disease Stomatognathic Diseases Disease or Syndrome 32 1 0.010 None 1.000 1 2017 2017
CUI: C0023223
Disease: Leg Ulcer
Leg Ulcer 		disease Skin and Connective Tissue Diseases Disease or Syndrome 40 0.010 None 1.000 1 2006 2006
CUI: C0871388
Disease: social stress
social stress 		disease Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 45 22 0.010 None 1.000 1 2017 2017
CUI: C0220704
Disease: Shprintzen syndrome
Shprintzen syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 46 3 0.010 None 1.000 1 1997 1997
CUI: C0025568
Disease: Metaplasia
Metaplasia 		phenotype Pathological Conditions, Signs and Symptoms Cell or Molecular Dysfunction 52 0.010 None 1.000 1 2006 2006
CUI: C0085083
Disease: Ovarian Hyperstimulation Syndrome
Ovarian Hyperstimulation Syndrome 		disease Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Disease or Syndrome 64 24 0.010 None 1.000 1 2017 2017
CUI: C0677055
Disease: CARCINOMA OF VULVA
CARCINOMA OF VULVA 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 72 2 0.010 None < 0.001 1 2012 2012
CUI: C0393819
Disease: Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating 		disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 82 4 0.020 None 1.000 2 2004 2018
CUI: C1997217
Disease: Low grade glioma
Low grade glioma 		disease Neoplasms Neoplastic Process 85 10 0.010 None < 0.001 1 2018 2018
CUI: C4721773
Disease: Postoperative cognitive dysfunction
Postoperative cognitive dysfunction 		phenotype Mental or Behavioral Dysfunction 93 0.010 None 1.000 1 2018 2018
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
AURAL ATRESIA, CONGENITAL 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 110 29 0.010 None 1.000 1 2018 2018
CUI: C0338508
Disease: Optic Atrophy 1
Optic Atrophy 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases Disease or Syndrome 117 45 0.010 None 1.000 1 2019 2019
CUI: C2919945
Disease: Cavernous Hemangioma of Brain
Cavernous Hemangioma of Brain 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Anatomical Abnormality 127 43 0.010 None 1.000 1 2011 2011
CUI: C0278874
Disease: Adult Ependymoma
Adult Ependymoma 		disease Neoplasms Neoplastic Process 144 3 0.010 None 1.000 1 2017 2017
CUI: C0796611
Disease: Newly Diagnosed Childhood Ependymoma
Newly Diagnosed Childhood Ependymoma 		disease Neoplasms Neoplastic Process 144 3 0.010 None 1.000 1 2017 2017
CUI: C0740392
Disease: Infarction, Middle Cerebral Artery
Infarction, Middle Cerebral Artery 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 145 0.200 None 1.000 1 2014 2014