F9, coagulation factor IX, 2158

N. diseases: 276; N. variants: 99
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: C2749016
Disease: Thrombophilia, X-Linked, Due To Factor Ix Defect
Thrombophilia, X-Linked, Due To Factor Ix Defect 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 1 5 0.700 strong 1.000 14 5 1989 2018
CUI: C1096488
Disease: Hereditary factor IX deficiency disease without inhibitor
Hereditary factor IX deficiency disease without inhibitor 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 1 0.010 None 1.000 1 1986 1986
CUI: C3494186
Disease: Autosomal Hemophilia A
Autosomal Hemophilia A 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 2 0.300 None 1.000 1 2005 2005
CUI: C0151563
Disease: Prolonged whole-blood clotting time
Prolonged whole-blood clotting time 		phenotype Hemic and Lymphatic Diseases Finding 4 0.100 None 0
CUI: C4023610
Disease: Abnormality of the intrinsic pathway
Abnormality of the intrinsic pathway 		phenotype Hemic and Lymphatic Diseases Anatomical Abnormality 4 0.100 None 0
CUI: C0015519
Disease: Factor X Deficiency
Factor X Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 5 27 0.010 None 1.000 1 2008 2008
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 5 0.010 None 1.000 1 2001 2001
CUI: C4023159
Disease: Reduced factor IX activity
Reduced factor IX activity 		phenotype Finding 5 0.100 None 0
CUI: C4321502
Disease: Factor XI Deficiency
Factor XI Deficiency 		disease Disease or Syndrome 6 9 0.010 None 1.000 1 2004 2004
CUI: C0750384
Disease: Coumarin Resistance
Coumarin Resistance 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 6 10 0.300 None 0
CUI: C0015523
Disease: Hereditary Factor XI Deficiency
Hereditary Factor XI Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 7 119 0.020 None 1.000 2 2004 2005
CUI: C0749424
Disease: Thyroid Hurthle Cell Carcinoma
Thyroid Hurthle Cell Carcinoma 		disease Neoplasms; Endocrine System Diseases Neoplastic Process 8 1 0.010 None 1.000 1 2015 2015
CUI: C0751156
Disease: FRAXA Syndrome
FRAXA Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 8 1 0.010 None 1.000 1 1991 1991
CUI: C3875007
Disease: Nodular thyroid disease
Nodular thyroid disease 		disease Endocrine System Diseases Disease or Syndrome 8 0.010 None 1.000 1 2000 2000
CUI: C4049005
Disease: Cataract, total congenital with posterior sutural opacities in Heterozygotes
Cataract, total congenital with posterior sutural opacities in Heterozygotes 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Congenital Abnormality 8 0.010 None 1.000 1 1998 1998
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 9 0.010 None 1.000 1 2006 2006
CUI: C3494187
Disease: Factor VIII Deficiency
Factor VIII Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 9 1 0.300 None 1.000 1 2005 2005
CUI: C1844374
Disease: Persistent bleeding after trauma
Persistent bleeding after trauma 		phenotype Finding 9 0.100 None 0
CUI: C0015503
Disease: Factor VII Deficiency
Factor VII Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 10 73 0.010 None 1.000 1 2000 2000
CUI: C4727087
Disease: Metastatic Lung Carcinoma
Metastatic Lung Carcinoma 		disease Neoplastic Process 10 0.010 None 1.000 1 2018 2018
CUI: C0027666
Disease: Neoplasms, Radiation-Induced
Neoplasms, Radiation-Induced 		phenotype Neoplasms; Wounds and Injuries Neoplastic Process 11 0.030 None 1.000 3 2001 2004
CUI: C0272324
Disease: Mild hereditary factor VIII deficiency disease
Mild hereditary factor VIII deficiency disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 11 6 0.020 None 1.000 2 2 2016 2020
CUI: C1336750
Disease: Thyroid Gland Oncocytic Adenoma
Thyroid Gland Oncocytic Adenoma 		disease Neoplasms; Endocrine System Diseases Neoplastic Process 11 0.010 None 1.000 1 2017 2017
CUI: C4287590
Disease: Thyroid Gland Noninvasive Follicular Neoplasm with Papillary-Like Nuclear Features
Thyroid Gland Noninvasive Follicular Neoplasm with Papillary-Like Nuclear Features 		disease Neoplasms; Endocrine System Diseases Neoplastic Process 13 5 0.070 None 1.000 7 2017 2020
CUI: C0040250
Disease: Tinea Capitis
Tinea Capitis 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 13 0.010 None 1.000 1 2004 2004