FGF21, fibroblast growth factor 21, 26291

N. diseases: 236; N. variants: 2
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: C0406607
Disease: Insulin lipoatrophy
Insulin lipoatrophy
disease Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Acquired Abnormality 1 0.010 None 1.000 1 2013 2013
CUI: C0270951
Disease: Ocular muscular dystrophy
Ocular muscular dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 3 1 0.010 None 1.000 1 2017 2017
CUI: C4087291
Disease: Cardiac steatosis
Cardiac steatosis
disease Cardiovascular Diseases Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C3888890
Disease: Polyuria-polydipsia syndrome
Polyuria-polydipsia syndrome
disease Disease or Syndrome 4 0.010 None 1.000 1 2018 2018
CUI: C0853892
Disease: Catabolic state
Catabolic state
phenotype Disease or Syndrome 8 0.010 None 1.000 1 2020 2020
CUI: C3888506
Disease: LDLR mutation
LDLR mutation
disease Congenital Abnormality 10 21 0.010 None 1.000 1 2015 2015
Carnitine palmitoyl transferase 2 deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 11 29 0.010 None < 0.001 1 2019 2019
CUI: C1740787
Disease: Cardiac autonomic neuropathy
Cardiac autonomic neuropathy
disease Nervous System Diseases Disease or Syndrome 11 1 0.010 None < 0.001 1 2017 2017
CUI: C2609315
Disease: Retinal angiomatous proliferation
Retinal angiomatous proliferation
disease Disease or Syndrome 12 4 0.010 None 1.000 1 2017 2017
CUI: C3554224
Disease: LEPTIN DEFICIENCY OR DYSFUNCTION
LEPTIN DEFICIENCY OR DYSFUNCTION
disease Disease or Syndrome 15 3 0.010 None 1.000 1 2015 2015
CUI: C4055183
Disease: Contrast - Induced Nephropathy
Contrast - Induced Nephropathy
disease Disease or Syndrome 19 0.010 None 1.000 1 2018 2018
CUI: C0038441
Disease: Stress Disorders, Traumatic
Stress Disorders, Traumatic
group Mental Disorders Mental or Behavioral Dysfunction 20 0.010 None 1.000 1 2017 2017
CUI: C0238284
Disease: Acute mountain sickness
Acute mountain sickness
disease Respiratory Tract Diseases Disease or Syndrome 21 3 0.010 None 1.000 1 2019 2019
Mastitis-metritis-agalactia syndrome
disease Female Urogenital Diseases and Pregnancy Complications; Infections; Skin and Connective Tissue Diseases Disease or Syndrome 23 3 0.020 None 1.000 2 2018 2018
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement
phenotype Laboratory Procedure 23 33 0.100 None 1.000 1 1 2013 2013
CUI: C0338430
Disease: Limbic Encephalitis
Limbic Encephalitis
disease Neoplasms; Infections; Nervous System Diseases Disease or Syndrome 27 0.010 None 1.000 1 2019 2019
CUI: C0746556
Disease: metabolic disturbance
metabolic disturbance
disease Disease or Syndrome 29 4 0.020 None 1.000 2 2016 2018
CUI: C0152105
Disease: Hypertensive heart disease
Hypertensive heart disease
disease Cardiovascular Diseases Disease or Syndrome 32 0.010 None 1.000 1 2019 2019
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 35 3 0.010 None 1.000 1 2012 2012
CUI: C0238281
Disease: Middle Cerebral Artery Syndrome
Middle Cerebral Artery Syndrome
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 35 0.300 None 1.000 1 2014 2014
CUI: C0740376
Disease: Middle Cerebral Artery Thrombosis
Middle Cerebral Artery Thrombosis
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 35 0.300 None 1.000 1 2014 2014
CUI: C0751845
Disease: Middle Cerebral Artery Embolus
Middle Cerebral Artery Embolus
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 35 0.300 None 1.000 1 2014 2014
Left Middle Cerebral Artery Infarction
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 35 0.300 None 1.000 1 2014 2014
Embolic Infarction, Middle Cerebral Artery
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 35 0.300 None 1.000 1 2014 2014
Thrombotic Infarction, Middle Cerebral Artery
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 35 0.300 None 1.000 1 2014 2014