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: C3278211
Disease: THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT 		disease Disease or Syndrome 1 38 0.600 strong 1.000 35 38 1994 2016
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		phenotype Neoplastic Process 6626 169 0.100 None 0.870 23 2003 2019
CUI: C4721208
Disease: Metastatic castration-resistant prostate cancer
Metastatic castration-resistant prostate cancer 		disease Neoplastic Process 140 2 0.100 None 0.941 17 2012 2020
CUI: C1282496
Disease: Metastasis from malignant tumor of prostate
Metastasis from malignant tumor of prostate 		disease Neoplastic Process 342 18 0.090 None 1.000 9 1999 2019
CUI: C1739135
Disease: Progression of prostate cancer
Progression of prostate cancer 		disease Neoplastic Process 398 7 0.050 None 0.800 5 2008 2020
CUI: C3281092
Disease: THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE 		disease Disease or Syndrome 1 6 0.600 strong 1.000 5 6 1995 2012
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		disease Disease or Syndrome 1075 276 0.020 None 1.000 2 2000 2007
CUI: C2586160
Disease: Homozygous protein S deficiency
Homozygous protein S deficiency 		disease Disease or Syndrome 1 1 0.020 None 1.000 2 1 1994 2010
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		disease Disease or Syndrome 3 1 0.020 None 1.000 2 2005 2011
CUI: C3714948
Disease: PACHYONYCHIA CONGENITA 3
PACHYONYCHIA CONGENITA 3 		disease Disease or Syndrome 209 20 0.020 None 1.000 2 2003 2010
CUI: C4725861
Disease: Metastatic Malignant Neoplasm in the Viscera
Metastatic Malignant Neoplasm in the Viscera 		disease Neoplastic Process 30 2 0.020 None 1.000 2 2019 2019
CUI: C0028259
Disease: Nodule
Nodule 		phenotype Acquired Abnormality 278 19 0.010 None 1.000 1 2017 2017
CUI: C0272138
Disease: Erythroblastosis
Erythroblastosis 		disease Disease or Syndrome 89 0.010 None 1.000 1 2008 2008
CUI: C0332853
Disease: Anastomosis
Anastomosis 		disease Acquired Abnormality 155 2 0.010 None 1.000 1 2003 2003
CUI: C0424139
Disease: Anxiety and fear
Anxiety and fear 		disease Mental or Behavioral Dysfunction 51 0.010 None 1.000 1 2017 2017
CUI: C0521158
Disease: Recurrent tumor
Recurrent tumor 		phenotype Neoplastic Process 735 33 0.010 None < 0.001 1 2018 2018
CUI: C0677944
Disease: Sentinel node (disorder)
Sentinel node (disorder) 		disease Disease or Syndrome 130 5 0.010 None 1.000 1 2005 2005
CUI: C1402294
Disease: Primary Lesion
Primary Lesion 		phenotype Disease or Syndrome 71 8 0.010 None 1.000 1 2017 2017
CUI: C1654637
Disease: androgen independent prostate cancer
androgen independent prostate cancer 		disease Neoplastic Process 190 5 0.010 None < 0.001 1 2005 2005
CUI: C1840264
Disease: IMMUNE SUPPRESSION
IMMUNE SUPPRESSION 		phenotype Disease or Syndrome 222 3 0.010 None 1.000 1 2018 2018
CUI: C1861696
Disease: EAR WAX, WET/DRY
EAR WAX, WET/DRY 		disease Disease or Syndrome 6 1 0.010 None 1.000 1 2018 2018
CUI: C2945759
Disease: aggressive cancer
aggressive cancer 		phenotype Neoplastic Process 83 5 0.010 None 1.000 1 2018 2018
CUI: C4025284
Disease: Reduced protein S activity
Reduced protein S activity 		phenotype Finding 2 3 0.100 None 1.000 1 3 2019 2019
CUI: C4727179
Disease: Castration-Sensitive Prostate Carcinoma
Castration-Sensitive Prostate Carcinoma 		disease Neoplastic Process 9 0.010 None 1.000 1 2009 2009
CUI: C4744712
Disease: Advanced Prostate Carcinoma
Advanced Prostate Carcinoma 		disease Neoplastic Process 9 0.010 None 1.000 1 2004 2004