PROS1, protein S, 5627

N. diseases: 283; N. variants: 57
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: C1623038
Disease: Cirrhosis
Cirrhosis
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 919 110 0.010 None < 0.001 1 2013 2013
CUI: C0042029
Disease: Urinary tract infection
Urinary tract infection
group Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 219 14 0.010 None 1.000 1 2018 2018
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids
group Neoplasms Neoplastic Process 569 154 0.010 None 1.000 1 2018 2018
CUI: C0042373
Disease: Vascular Diseases
Vascular Diseases
group Cardiovascular Diseases Disease or Syndrome 688 40 0.010 None 1.000 1 2017 2017
CUI: C0558353
Disease: Tongue Carcinoma
Tongue Carcinoma
disease Neoplasms; Stomatognathic Diseases Neoplastic Process 157 2 0.010 None < 0.001 1 2015 2015
CUI: C0949664
Disease: Tauopathies
Tauopathies
group Nervous System Diseases Disease or Syndrome 245 43 0.010 None 1.000 1 2006 2006
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 15 7 0.010 None 1.000 1 2015 2015
CUI: C0085278
Disease: Antiphospholipid Syndrome
Antiphospholipid Syndrome
disease Immune System Diseases Disease or Syndrome 99 17 0.010 None 1.000 1 2012 2012
CUI: C0085409
Disease: Polyendocrinopathies, Autoimmune
Polyendocrinopathies, Autoimmune
group Immune System Diseases; Endocrine System Diseases Disease or Syndrome 166 21 0.010 None 1.000 1 1 2012 2012
CUI: C0086692
Disease: Benign Neoplasm
Benign Neoplasm
group Neoplasms Neoplastic Process 371 7 0.010 None 1.000 1 2005 2005
CUI: C0919890
Disease: Hyperfibrinogenemia
Hyperfibrinogenemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 9 1 0.010 None 1.000 1 2011 2011
CUI: C0878773
Disease: Overactive Bladder
Overactive Bladder
disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 65 3 0.010 None 1.000 1 2017 2017
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
group Nervous System Diseases Disease or Syndrome 512 264 0.010 None 1.000 1 2018 2018
CUI: C0858252
Disease: Breast adenocarcinoma
Breast adenocarcinoma
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 219 7 0.010 None < 0.001 1 2004 2004
CUI: C0796149
Disease: Scott Syndrome
Scott Syndrome
disease Hemic and Lymphatic Diseases Disease or Syndrome 15 0.010 None 1.000 1 2016 2016
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 14 9 0.010 None 1.000 1 2015 2015
CUI: C0153349
Disease: Malignant neoplasm of tongue
Malignant neoplasm of tongue
disease Neoplasms; Stomatognathic Diseases Neoplastic Process 155 1 0.010 None < 0.001 1 2015 2015
CUI: C0751571
Disease: Cancer of Urinary Tract
Cancer of Urinary Tract
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 65 11 0.010 None 1.000 1 2017 2017
CUI: C0040822
Disease: Tremor
Tremor
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 528 52 0.010 None 1.000 1 2019 2019
CUI: C1096063
Disease: Drug Resistant Epilepsy
Drug Resistant Epilepsy
disease Nervous System Diseases Disease or Syndrome 184 35 0.010 None 1.000 1 2017 2017
CUI: C0033626
Disease: Protein Deficiency
Protein Deficiency
disease Nutritional and Metabolic Diseases Disease or Syndrome 125 2 0.010 None 1.000 1 1988 1988
CUI: C0041948
Disease: Uremia
Uremia
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 110 2 0.010 None 1.000 1 2005 2005
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
group Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 2780 385 0.010 None 1.000 1 1999 1999
CUI: C0034902
Disease: Pure Red-Cell Aplasia
Pure Red-Cell Aplasia
disease Hemic and Lymphatic Diseases Disease or Syndrome 49 7 0.010 None 1.000 1 2008 2008
CUI: C1402294
Disease: Primary Lesion
Primary Lesion
phenotype Disease or Syndrome 71 8 0.010 None 1.000 1 2017 2017