TIMELESS, timeless circadian regulator, 8914

N. diseases: 140; N. variants: 24
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: C0429494
Disease: Ocular axial length
Ocular axial length 		phenotype Clinical Attribute 4 11 0.100 None 1.000 1 1 2013 2013
CUI: C0581874
Disease: Late insomnia
Late insomnia 		phenotype Nervous System Diseases; Mental Disorders Mental or Behavioral Dysfunction 4 1 0.010 None 1.000 1 2009 2009
CUI: C0854739
Disease: Advanced sleep phase
Advanced sleep phase 		phenotype Disease or Syndrome 5 1 0.010 None 1.000 1 2019 2019
CUI: C0859021
Disease: Hyperthymic state
Hyperthymic state 		disease Mental or Behavioral Dysfunction 8 5 0.010 None 1.000 1 2 2017 2017
CUI: C0541798
Disease: Early Awakening
Early Awakening 		phenotype Nervous System Diseases; Mental Disorders Mental or Behavioral Dysfunction 10 1 0.010 None 1.000 1 2010 2010
CUI: C0860027
Disease: Leishmania infantum disease
Leishmania infantum disease 		disease Disease or Syndrome 11 0.010 None 1.000 1 2018 2018
CUI: C0744421
Disease: Immune-complex glomerulonephritis
Immune-complex glomerulonephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 12 0.010 None 1.000 1 2019 2019
CUI: C0242917
Disease: Filoviridae Infections
Filoviridae Infections 		disease Infections Disease or Syndrome 13 0.010 None 1.000 1 2014 2014
CUI: C1276071
Disease: Childhood atopic dermatitis
Childhood atopic dermatitis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 13 0.010 None 1.000 1 2006 2006
CUI: C0268314
Disease: Cholestasis-edema syndrome, Norwegian type
Cholestasis-edema syndrome, Norwegian type 		disease Digestive System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 14 0.010 None 1.000 1 2013 2013
CUI: C1332629
Disease: Breast Fibrocystic Change, Proliferative Type
Breast Fibrocystic Change, Proliferative Type 		disease Skin and Connective Tissue Diseases Disease or Syndrome 14 0.010 None 1.000 1 2004 2004
CUI: C3825816
Disease: Pneumonia in children
Pneumonia in children 		disease Disease or Syndrome 15 3 0.010 None 1.000 1 2020 2020
CUI: C0947961
Disease: Atopic disorders
Atopic disorders 		group Disease or Syndrome 29 2 0.010 None 1.000 1 2007 2007
CUI: C0340164
Disease: Lofgrens syndrome
Lofgrens syndrome 		disease Hemic and Lymphatic Diseases Disease or Syndrome 30 13 0.010 None 1.000 1 2009 2009
CUI: C0948216
Disease: Ovarian adenocarcinoma
Ovarian adenocarcinoma 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Neoplastic Process 43 1 0.010 None 1.000 1 2016 2016
CUI: C0947785
Disease: [D]Sleep disturbances (& [hypersomnia] or [insomnia])
[D]Sleep disturbances (& [hypersomnia] or [insomnia]) 		phenotype Sign or Symptom 69 23 0.010 None 1.000 1 1 2016 2016
CUI: C0694549
Disease: Community acquired pneumonia
Community acquired pneumonia 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 75 13 0.010 None 1.000 1 2020 2020
CUI: C0403416
Disease: Idiopathic crescentic glomerulonephritis
Idiopathic crescentic glomerulonephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 80 0.010 None 1.000 1 2015 2015
CUI: C0020651
Disease: Hypotension, Orthostatic
Hypotension, Orthostatic 		phenotype Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 82 21 0.010 None 1.000 1 2018 2018
CUI: C0032231
Disease: Pleurisy
Pleurisy 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 82 7 0.010 None 1.000 1 2019 2019
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		phenotype Laboratory Procedure 82 123 0.100 None 1.000 1 1 2012 2012
CUI: C0853193
Disease: Bipolar I disorder
Bipolar I disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 83 46 0.010 None 1.000 1 2006 2006
CUI: C0796074
Disease: MOHR-TRANEBJAERG SYNDROME
MOHR-TRANEBJAERG SYNDROME 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms Disease or Syndrome 89 19 0.010 None 1.000 1 2000 2000
CUI: C0919747
Disease: Cytokine storm
Cytokine storm 		disease Disease or Syndrome 97 0.020 None 1.000 2 2017 2019
CUI: C0002382
Disease: Alveolar Bone Loss
Alveolar Bone Loss 		disease Musculoskeletal Diseases; Stomatognathic Diseases Disease or Syndrome 101 0.010 None 1.000 1 2017 2017