CHI3L1, chitinase 3 like 1, 1116

N. diseases: 420; N. variants: 9
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: C1997728
Disease: Osteomyelitis due to Staphylococcus aureus
Osteomyelitis due to Staphylococcus aureus 		disease Infections Disease or Syndrome 1 0.010 None 1.000 1 2015 2015
CUI: C2677770
Disease: ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7 		phenotype Finding 1 1 0.300 None 0 1
CUI: C0262585
Disease: ONYCHOPATHY
ONYCHOPATHY 		disease Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C4024843
Disease: Late onset atopic dermatitis
Late onset atopic dermatitis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 2 0.010 None 1.000 1 2017 2017
CUI: C1868833
Disease: Bronchial wall thickening
Bronchial wall thickening 		disease Disease or Syndrome 5 0.010 None 1.000 1 2013 2013
CUI: C0005750
Disease: Blind Loop Syndrome
Blind Loop Syndrome 		disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 6 3 0.010 None 1.000 1 2017 2017
CUI: C3828464
Disease: Proneural Glioblastoma
Proneural Glioblastoma 		disease Neoplastic Process 7 0.010 None 1.000 1 2018 2018
CUI: C4324721
Disease: Radiologically isolated syndrome
Radiologically isolated syndrome 		disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 8 0.020 None 1.000 2 2018 2019
CUI: C3875265
Disease: Febrile urinary tract infection
Febrile urinary tract infection 		disease Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 8 2 0.010 None 1.000 1 2018 2018
CUI: C0268468
Disease: Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency
Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Behavior and Behavior Mechanisms Disease or Syndrome 10 9 0.010 None 1.000 1 2019 2019
CUI: C0001311
Disease: Acute bronchiolitis
Acute bronchiolitis 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 11 3 0.010 None 1.000 1 2017 2017
CUI: C0154822
Disease: Serous retinal detachment
Serous retinal detachment 		disease Eye Diseases Disease or Syndrome 12 2 0.010 None 1.000 1 2019 2019
CUI: C0272236
Disease: Hyperimmunoglobulin M syndrome
Hyperimmunoglobulin M syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 12 1 0.010 None 1.000 1 1993 1993
CUI: C0027562
Disease: Negativism
Negativism 		phenotype Behavior and Behavior Mechanisms Individual Behavior 12 0.100 None 0
CUI: C3805054
Disease: Prodromal Alzheimer's disease
Prodromal Alzheimer's disease 		disease Mental or Behavioral Dysfunction 13 2 0.020 None 1.000 2 2014 2020
CUI: C0032310
Disease: Pneumonia, Viral
Pneumonia, Viral 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 13 1 0.010 None 1.000 1 2018 2018
CUI: C1112433
Disease: Thromboembolic stroke
Thromboembolic stroke 		disease Cardiovascular Diseases Disease or Syndrome 13 1 0.010 None 1.000 1 2014 2014
CUI: C1866986
Disease: Social and occupational deterioration
Social and occupational deterioration 		phenotype Mental Disorders Finding 13 0.100 None 0
CUI: C0340569
Disease: Internal Carotid Artery Stenosis
Internal Carotid Artery Stenosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 15 0.010 None 1.000 1 2017 2017
CUI: C3825816
Disease: Pneumonia in children
Pneumonia in children 		disease Disease or Syndrome 15 3 0.010 None 1.000 1 2018 2018
CUI: C0543698
Disease: Hypersensitive syndrome
Hypersensitive syndrome 		disease Immune System Diseases Disease or Syndrome 17 2 0.010 None 1.000 1 2020 2020
CUI: C1303258
Disease: Acute ST segment elevation myocardial infarction (disorder)
Acute ST segment elevation myocardial infarction (disorder) 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 17 0.010 None 1.000 1 2019 2019
CUI: C4739246
Disease: Apnea+hypopnea
Apnea+hypopnea 		disease Disease or Syndrome 17 3 0.010 None 1.000 1 2017 2017
CUI: C0428974
Disease: Supraventricular arrhythmia
Supraventricular arrhythmia 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 19 2 0.010 None 1.000 1 2017 2017
CUI: C1864389
Disease: PREMATURE CHROMATID SEPARATION TRAIT
PREMATURE CHROMATID SEPARATION TRAIT 		disease Disease or Syndrome 19 10 0.010 None 1.000 1 2017 2017