CSF3, colony stimulating factor 3, 1440

N. diseases: 687; N. variants: 4
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: C0423618
Disease: Throbbing Headache
Throbbing Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.300 None 1.000 1 2000 2000
CUI: C0423623
Disease: Bilateral Headache
Bilateral Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.300 None 1.000 1 2000 2000
CUI: C0426576
Disease: Gastrointestinal symptom
Gastrointestinal symptom 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 69 7 0.010 None 1.000 1 2019 2019
CUI: C0474366
Disease: Generalized Headache
Generalized Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.300 None 1.000 1 2000 2000
CUI: C0542476
Disease: Forgetful
Forgetful 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Sign or Symptom 429 18 0.010 None 1.000 1 2011 2011
CUI: C0751186
Disease: Orthostatic Headache
Orthostatic Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 7 0.300 None 1.000 1 2000 2000
CUI: C0751187
Disease: Periorbital Headache
Periorbital Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.300 None 1.000 1 2000 2000
CUI: C0751189
Disease: Retro-Ocular Headache
Retro-Ocular Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.300 None 1.000 1 2000 2000
CUI: C0751190
Disease: Sharp Headache
Sharp Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.300 None 1.000 1 2000 2000
CUI: C0751192
Disease: Vertex Headache
Vertex Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.300 None 1.000 1 2000 2000
CUI: C0752255
Disease: Impairment, Light Touch Sensation
Impairment, Light Touch Sensation 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 2 0.300 None 1.000 1 1995 1995
CUI: C0752256
Disease: Pain Sensation Diminished
Pain Sensation Diminished 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 2 0.300 None 1.000 1 1995 1995
CUI: C0752257
Disease: Pinprick Sensation Diminished
Pinprick Sensation Diminished 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 2 0.300 None 1.000 1 1995 1995
CUI: C0752260
Disease: Proprioceptive Disorders
Proprioceptive Disorders 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 2 0.300 None 1.000 1 1995 1995
CUI: C0877781
Disease: Hemicrania
Hemicrania 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 1 0.300 None 1.000 1 2000 2000
CUI: C0920289
Disease: Sluggishness
Sluggishness 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Sign or Symptom 2 0.010 None 1.000 1 2017 2017
CUI: C0948775
Disease: High weight
High weight 		phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Sign or Symptom 12 0.010 None 1.000 1 2017 2017
CUI: C2936719
Disease: Mechanical Allodynia
Mechanical Allodynia 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 408 4 0.010 None 1.000 1 2019 2019
CUI: C3714772
Disease: Recurrent fevers
Recurrent fevers 		phenotype Sign or Symptom 48 4 0.010 None 1.000 1 2017 2017
CUI: C0016059
Disease: Fibrosis
Fibrosis 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 184 0.300 None 1.000 2 2009 2010
CUI: C0041755
Disease: Adverse reaction to drug
Adverse reaction to drug 		group Chemically-Induced Disorders Pathologic Function 87 0.300 None 1.000 2 1993 2016
CUI: C0242698
Disease: Ventricular Dysfunction, Left
Ventricular Dysfunction, Left 		phenotype Cardiovascular Diseases Pathologic Function 88 0.300 None 1.000 2 2003 2007
CUI: C0333355
Disease: Inflammatory disease of mucous membrane
Inflammatory disease of mucous membrane 		group Digestive System Diseases; Stomatognathic Diseases Pathologic Function 18 0.300 None 1.000 2 1995 2006
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion 		phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function 188 0.300 None 1.000 1 2008 2008
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal 		phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function 109 0.300 None 1.000 1 2008 2008