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.
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		disease Digestive System Diseases Disease or Syndrome 1458 827 0.010 None 1.000 1 2020 2020
CUI: C0013146
Disease: Drug abuse
Drug abuse 		group Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 405 39 0.010 None 1.000 1 2020 2020
CUI: C0015672
Disease: Fatigue
Fatigue 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 760 67 0.010 None 1.000 1 2020 2020
CUI: C0024291
Disease: Lymphohistiocytosis, Hemophagocytic
Lymphohistiocytosis, Hemophagocytic 		disease Hemic and Lymphatic Diseases Disease or Syndrome 117 13 0.010 None 1.000 1 2020 2020
CUI: C0025007
Disease: Measles
Measles 		disease Infections Disease or Syndrome 113 6 0.010 None 1.000 1 2020 2020
CUI: C0033797
Disease: Pseudodementia
Pseudodementia 		disease Mental Disorders Mental or Behavioral Dysfunction 3 0.010 None 1.000 1 2020 2020
CUI: C0038506
Disease: Stuttering
Stuttering 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Mental or Behavioral Dysfunction 34 8 0.010 None 1.000 1 2020 2020
CUI: C0038538
Disease: Subdural Effusion
Subdural Effusion 		phenotype Infections; Nervous System Diseases Acquired Abnormality 2 0.010 None 1.000 1 2020 2020
CUI: C0041341
Disease: Tuberous Sclerosis
Tuberous Sclerosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases Neoplastic Process 289 55 0.010 None 1.000 1 2020 2020
CUI: C0086647
Disease: Mucopolysaccharidosis Type IIIA
Mucopolysaccharidosis Type IIIA 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 25 69 0.010 None 1.000 1 2020 2020
CUI: C0162835
Disease: Hypopigmentation disorder
Hypopigmentation disorder 		disease Skin and Connective Tissue Diseases Disease or Syndrome 126 15 0.010 None 1.000 1 2020 2020
CUI: C0238378
Disease: Desquamative interstitial pneumonia
Desquamative interstitial pneumonia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases Disease or Syndrome 9 1 0.010 None 1.000 1 2020 2020
CUI: C0497299
Disease: meningitis/encephalitis
meningitis/encephalitis 		disease Disease or Syndrome 5 0.010 None 1.000 1 2020 2020
CUI: C1876214
Disease: ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT
ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 54 6 0.010 None 1.000 1 2020 2020
CUI: C2921627
Disease: Clinically isolated syndrome
Clinically isolated syndrome 		disease Disease or Syndrome 54 2 0.040 None 1.000 4 2019 2019
CUI: C0233794
Disease: Memory impairment
Memory impairment 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 763 48 0.030 None 1.000 3 2019 2019
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 0.030 None 1.000 3 2019 2019
CUI: C0751188
Disease: Post-Dural Puncture Headaches
Post-Dural Puncture Headaches 		phenotype Nervous System Diseases Sign or Symptom 2 0.030 None 1.000 3 2019 2019
CUI: C3811918
Disease: GRN-related frontotemporal dementia
GRN-related frontotemporal dementia 		disease Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders Disease or Syndrome 112 20 0.030 None 1.000 3 2019 2020
CUI: C4543926
Disease: Narcolepsy type 1
Narcolepsy type 1 		disease Nervous System Diseases; Mental Disorders Disease or Syndrome 35 0.030 None 1.000 3 2019 2020
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 488 90 0.020 None 1.000 2 2019 2019
CUI: C0014059
Disease: Encephalomyelitis, Acute Disseminated
Encephalomyelitis, Acute Disseminated 		disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 24 0.020 None 1.000 2 2019 2019
CUI: C0019340
Disease: Herpes NOS
Herpes NOS 		disease Infections Disease or Syndrome 114 5 0.020 None 1.000 2 2019 2020
CUI: C0085632
Disease: Apathy
Apathy 		phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 83 9 0.020 None 1.000 2 2019 2019
CUI: C0220654
Disease: Meningeal Carcinomatosis
Meningeal Carcinomatosis 		disease Neoplasms; Nervous System Diseases Neoplastic Process 14 1 0.020 None 1.000 2 2019 2019