GC, GC vitamin D binding protein, 2638

N. diseases: 219; N. variants: 17
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: C0262565
Disease: Anteroseptal Myocardial Infarction
Anteroseptal Myocardial Infarction 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 1 1 0.010 None 1.000 1 1 2019 2019
CUI: C0858312
Disease: Mycobacterium tuberculosis meningitis
Mycobacterium tuberculosis meningitis 		disease Infections; Nervous System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C1832465
Disease: Atrophia Maculosa Varioliformis Cutis, Familial
Atrophia Maculosa Varioliformis Cutis, Familial 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 1 1 0.010 None 1.000 1 1 2019 2019
CUI: C1168279
Disease: Melalgia
Melalgia 		phenotype Sign or Symptom 2 0.010 None 1.000 1 2014 2014
CUI: C2945566
Disease: Chronic mucus hypersecretion
Chronic mucus hypersecretion 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 3 1 0.010 None 1.000 1 2004 2004
CUI: C0005716
Disease: Blastomycosis
Blastomycosis 		disease Infections; Skin and Connective Tissue Diseases; Respiratory Tract Diseases Disease or Syndrome 5 0.010 None 1.000 1 2014 2014
CUI: C0016395
Disease: Focal Dermal Hypoplasia
Focal Dermal Hypoplasia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 5 9 0.010 None 1.000 1 1995 1995
CUI: C0036981
Disease: Endotoxic shock
Endotoxic shock 		phenotype Pathological Conditions, Signs and Symptoms; Infections Pathologic Function 6 0.300 None 1.000 1 2007 2007
CUI: C0919718
Disease: Calcification of mitral valve
Calcification of mitral valve 		disease Disease or Syndrome 8 2 0.010 None 1.000 1 2019 2019
CUI: C0342185
Disease: Hyperthyroxinemia, Familial Dysalbuminemic
Hyperthyroxinemia, Familial Dysalbuminemic 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases Disease or Syndrome 12 4 0.010 None 1.000 1 1995 1995
CUI: C0751197
Disease: Fulminant Hepatic Failure with Cerebral Edema
Fulminant Hepatic Failure with Cerebral Edema 		disease Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 13 0.300 None 1.000 1 2001 2001
CUI: C0751198
Disease: Hepatic Stupor
Hepatic Stupor 		disease Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 13 0.300 None 1.000 1 2001 2001
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement 		phenotype Laboratory Procedure 14 51 0.100 None 1.000 7 6 2010 2018
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement 		phenotype Laboratory Procedure 14 51 0.100 None 1.000 7 6 2010 2018
CUI: C0019147
Disease: Hepatic Coma
Hepatic Coma 		disease Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 14 0.300 None 1.000 1 2001 2001
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 14 2 0.010 None 1.000 1 1990 1990
CUI: C2316786
Disease: Chronic kidney disease stage 2
Chronic kidney disease stage 2 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 15 1 0.010 None 1.000 1 2018 2018
CUI: C0699744
Disease: Infection of ear
Infection of ear 		group Otorhinolaryngologic Diseases Disease or Syndrome 16 0.010 None 1.000 1 2018 2018
CUI: C0085399
Disease: Ehrlichiosis
Ehrlichiosis 		disease Infections Disease or Syndrome 21 0.010 None 1.000 1 2017 2017
CUI: C0399447
Disease: Early onset periodontitis
Early onset periodontitis 		disease Stomatognathic Diseases Disease or Syndrome 21 0.010 None 1.000 1 1993 1993
CUI: C0238694
Disease: Peripheral arthritis
Peripheral arthritis 		disease Musculoskeletal Diseases Disease or Syndrome 22 15 0.010 None 1.000 1 3 2011 2011
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 23 168 0.010 None 1.000 1 1990 1990
CUI: C0878555
Disease: Diffuse panbronchiolitis
Diffuse panbronchiolitis 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 26 0.010 None < 0.001 1 2001 2001
CUI: C0865800
Disease: asthma with copd
asthma with copd 		disease Disease or Syndrome 29 0.010 None 1.000 1 2010 2010
CUI: C0007125
Disease: Carcinoma, Ehrlich Tumor
Carcinoma, Ehrlich Tumor 		disease Neoplasms Neoplastic Process; Experimental Model of Disease 30 0.010 None 1.000 1 1997 1997