CSF2, colony stimulating factor 2, 1437

N. diseases: 1028; N. variants: 7
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.
Fenestration (morphologic abnormality)
disease Acquired Abnormality 43 0.010 None 1.000 1 2017 2017
CUI: C0016427
Disease: Follicular cyst
Follicular cyst
disease Neoplasms Acquired Abnormality 4 0.010 None 1.000 1 1995 1995
CUI: C0038538
Disease: Subdural Effusion
Subdural Effusion
phenotype Infections; Nervous System Diseases Acquired Abnormality 2 0.010 None 1.000 1 2020 2020
CUI: C0242362
Disease: Disk, Herniated
Disk, Herniated
disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Acquired Abnormality 31 0.010 None 1.000 1 2017 2017
CUI: C0333161
Disease: Pseudocyst
Pseudocyst
disease Pathological Conditions, Signs and Symptoms; Neoplasms Acquired Abnormality 8 0.010 None 1.000 1 2017 2017
Hernia of cerebellar tonsil into foramen magnum
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Acquired Abnormality 3 0.010 None 1.000 1 2017 2017
CUI: C0740391
Disease: Middle Cerebral Artery Occlusion
Middle Cerebral Artery Occlusion
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 626 0.010 None 1.000 1 2018 2018
CUI: C1265713
Disease: Trephine hole
Trephine hole
disease Acquired Abnormality 5 0.010 None 1.000 1 2018 2018
CUI: C1515091
Disease: Surgically-Created Resection Cavity
Surgically-Created Resection Cavity
disease Acquired Abnormality 16 3 0.010 None 1.000 1 2017 2017
CUI: C0016169
Disease: pathologic fistula
pathologic fistula
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 71 8 0.100 None 0.800 10 2017 2019
CUI: C0039147
Disease: Syrinx formation
Syrinx formation
disease Anatomical Abnormality 18 0.020 None 1.000 2 2017 2019
CUI: C0019270
Disease: Hernia
Hernia
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 136 10 0.010 None 1.000 1 2019 2019
CUI: C0032584
Disease: polyps
polyps
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 390 18 0.010 None 1.000 1 1991 1991
CUI: C0269199
Disease: Stenosis of cervix
Stenosis of cervix
disease Female Urogenital Diseases and Pregnancy Complications Anatomical Abnormality 2 0.010 None 1.000 1 2018 2018
CUI: C0302142
Disease: Deformity
Deformity
group Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Anatomical Abnormality 350 26 0.010 None 1.000 1 2017 2017
CUI: C1510420
Disease: Cavitation
Cavitation
disease Anatomical Abnormality 47 0.010 None 1.000 1 2019 2019
CUI: C0750929
Disease: Arnold-Chiari Malformation, Type I
Arnold-Chiari Malformation, Type I
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 41 1 0.090 None 0.778 9 2017 2019
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 93 6 0.040 None 1.000 4 2018 2020
CUI: C0013589
Disease: Ectromelia
Ectromelia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 30 0.030 None 1.000 3 2017 2019
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 89 27 0.030 None 0.667 3 2018 2019
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 1098 73 0.020 None 1.000 2 2017 2019
CUI: C0027794
Disease: Neural Tube Defects
Neural Tube Defects
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 304 122 0.310 None 1.000 2 2006 2017
Congenital stenosis of aqueduct of Sylvius
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 6 0.020 None 0.500 2 2018 2019
CUI: C0340970
Disease: Congenital neutropenia
Congenital neutropenia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Congenital Abnormality 68 11 0.020 None 1.000 2 1993 2020
CUI: C4551722
Disease: Encephalocele
Encephalocele
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Nervous System Diseases Congenital Abnormality 23 7 0.020 None 1.000 2 2019 2020