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: C0423757
Disease: Thin skin
Thin skin
phenotype Finding 77 4 0.100 None 0
CUI: C1867638
Disease: Warfarin-induced skin necrosis
Warfarin-induced skin necrosis
phenotype Finding 2 0.100 None 0
CUI: C4553919
Disease: Superficial Thrombophlebitis, CTCAE
Superficial Thrombophlebitis, CTCAE
phenotype Finding 3 0.100 None 0
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation
phenotype Finding 58 5 0.100 None 0
CUI: C0040046
Disease: Thrombophlebitis
Thrombophlebitis
disease Cardiovascular Diseases Pathologic Function 3 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: C0042485
Disease: Venous Insufficiency
Venous Insufficiency
disease Cardiovascular Diseases Disease or Syndrome 17 1 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
Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Recessive
disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.300 None 0
Abnormality of the cerebral vasculature
disease Anatomical Abnormality 18 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: C0017086
Disease: Gangrene
Gangrene
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 69 4 0.100 None 0
Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant
disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.300 None 0
CUI: C1962966
Disease: Retinopathy, CTCAE
Retinopathy, CTCAE
phenotype Finding 108 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: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism
disease Respiratory Tract Diseases; Cardiovascular Diseases Pathologic Function 93 16 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: C0034150
Disease: Purpura
Purpura
disease Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 68 1 0.100 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: C0035309
Disease: Retinal Diseases
Retinal Diseases
group Eye Diseases Disease or Syndrome 714 56 0.100 None 0
Pyruvate Carboxylase Deficiency Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 14 33 0.090 None 1.000 9 1987 2018
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: C0398625
Disease: Protein C Deficiency
Protein C Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 43 14 0.010 None 1.000 1 1988 1988
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency
disease Hemic and Lymphatic Diseases Disease or Syndrome 19 14 0.400 strong 0.967 30 5 1989 2019
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary
disease Hemic and Lymphatic Diseases Disease or Syndrome 17 9 0.020 None 1.000 2 1 1989 2017