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: C0042485
Disease: Venous Insufficiency
Venous Insufficiency 		disease Cardiovascular Diseases Disease or Syndrome 17 1 0.100 None 0
CUI: C4022001
Disease: Abnormality of the cerebral vasculature
Abnormality of the cerebral vasculature 		disease Anatomical Abnormality 18 0.100 None 0
CUI: C0037299
Disease: Skin Ulcer
Skin Ulcer 		phenotype Skin and Connective Tissue Diseases Disease or Syndrome 151 1 0.100 None 0
CUI: C3890030
Disease: PROTEIN S HEERLEN PHENOTYPE
PROTEIN S HEERLEN PHENOTYPE 		phenotype Finding 1 1 0.100 None 0 1
CUI: C1962966
Disease: Retinopathy, CTCAE
Retinopathy, CTCAE 		phenotype Finding 108 0.100 None 0
CUI: C3502052
Disease: Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant
Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant 		disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.300 None 0
CUI: C3502051
Disease: Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Recessive
Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Recessive 		disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.300 None 0
CUI: C0456909
Disease: Blindness
Blindness 		phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 393 34 0.100 None 0
CUI: C0017086
Disease: Gangrene
Gangrene 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 69 4 0.100 None 0
CUI: C4553919
Disease: Superficial Thrombophlebitis, CTCAE
Superficial Thrombophlebitis, CTCAE 		phenotype Finding 3 0.100 None 0
CUI: C1867638
Disease: Warfarin-induced skin necrosis
Warfarin-induced skin necrosis 		phenotype Finding 2 0.100 None 0
CUI: C0040046
Disease: Thrombophlebitis
Thrombophlebitis 		disease Cardiovascular Diseases Pathologic Function 3 0.100 None 0
CUI: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism 		disease Respiratory Tract Diseases; Cardiovascular Diseases Pathologic Function 93 16 0.100 None 0
CUI: C0151942
Disease: Arterial thrombosis
Arterial thrombosis 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 33 1 0.100 None 0
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 122 78 0.100 None 0
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases 		group Eye Diseases Disease or Syndrome 714 56 0.100 None 0
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		disease Digestive System Diseases; Neoplasms Neoplastic Process 5473 1962 0.300 None 0 1
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation 		phenotype Finding 58 5 0.100 None 0
CUI: C0034150
Disease: Purpura
Purpura 		disease Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 68 1 0.100 None 0
CUI: C0423757
Disease: Thin skin
Thin skin 		phenotype Finding 77 4 0.100 None 0
CUI: C0558353
Disease: Tongue Carcinoma
Tongue Carcinoma 		disease Neoplasms; Stomatognathic Diseases Neoplastic Process 157 2 0.010 None < 0.001 1 2015 2015
CUI: C1851920
Disease: Dopa-Responsive Dystonia
Dopa-Responsive Dystonia 		disease Nervous System Diseases Disease or Syndrome 28 33 0.010 None < 0.001 1 2018 2018
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: C1623038
Disease: Cirrhosis
Cirrhosis 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 919 110 0.010 None < 0.001 1 2013 2013
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