F10, coagulation factor X, 2159

N. diseases: 228; N. variants: 44
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: C0018965
Disease: Hematuria
Hematuria
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 235 31 0.100 None 0
CUI: C0019065
Disease: Hemoperitoneum
Hemoperitoneum
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Pathologic Function 1 0.100 None 0
CUI: C4022608
Disease: Oral cavity bleeding
Oral cavity bleeding
phenotype Pathologic Function 18 0.100 None 0
CUI: C0240412
Disease: Muscle hematoma
Muscle hematoma
disease Pathological Conditions, Signs and Symptoms Injury or Poisoning 6 0.100 None 0
CUI: C1697453
Disease: Spontaneous hematomas
Spontaneous hematomas
disease Disease or Syndrome 33 0.100 None 0
CUI: C1861403
Disease: Variable expressivity
Variable expressivity
phenotype Finding 319 0.100 None 0
CUI: C0032797
Disease: Postpartum Hemorrhage
Postpartum Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Pathologic Function 6 0.100 None 0
CUI: C4021745
Disease: Abnormality of the musculature
Abnormality of the musculature
phenotype Anatomical Abnormality 24 0.100 None 0
CUI: C4024702
Disease: Reduced factor X activity
Reduced factor X activity
phenotype Finding 3 0.100 None 0
Partial thromboplastin time increased (finding)
phenotype Finding 18 1 0.100 None 0
Antepartum hemorrhage affecting fetus or newborn
phenotype Finding 1 0.100 None 0
CUI: C0017181
Disease: Gastrointestinal Hemorrhage
Gastrointestinal Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Pathologic Function 122 24 0.100 None 0
CUI: C4023145
Disease: Abnormal umbilical stump bleeding
Abnormal umbilical stump bleeding
disease Anatomical Abnormality 5 0.100 None 0
CUI: C0269608
Disease: Antepartum hemorrhage
Antepartum hemorrhage
phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function 1 0.100 None 0
CUI: C0014591
Disease: Epistaxis
Epistaxis
phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Pathologic Function 82 4 0.100 None 0
CUI: C4021646
Disease: Prolonged bleeding after surgery
Prolonged bleeding after surgery
phenotype Pathologic Function 11 0.100 None 0
CUI: C0423798
Disease: Increased tendency to bruise
Increased tendency to bruise
phenotype Wounds and Injuries Finding 133 14 0.100 None 0
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
group Neoplasms Neoplastic Process 8221 1374 0.090 None 0.889 9 2018 2019
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
group Neoplasms Neoplastic Process 8621 1641 0.090 None 0.889 9 2018 2019
CUI: C0027651
Disease: Neoplasms
Neoplasms
group Neoplasms Neoplastic Process 10161 1644 0.080 None 0.875 8 2005 2019
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 6385 327 0.060 None 1.000 6 2000 2019
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 41 30 0.060 None 1.000 6 1995 2017
Embolic stroke of undetermined source
disease Disease or Syndrome 4 0.050 None 1.000 5 2017 2019
CUI: C0684275
Disease: Hemophilia, NOS
Hemophilia, NOS
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 82 8 0.050 None 1.000 5 2011 2019
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
disease Cardiovascular Diseases Disease or Syndrome 2006 267 0.040 None 1.000 4 2002 2019