NPY, neuropeptide Y, 4852

N. diseases: 381; N. variants: 12
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: C4755308
Disease: Familial cervical artery dissection
Familial cervical artery dissection
disease Disease or Syndrome 9 2 0.010 None 1.000 1 2009 2009
CUI: C0262385
Disease: Autonomic nervous system imbalance
Autonomic nervous system imbalance
disease Nervous System Diseases Disease or Syndrome 11 0.010 None 1.000 1 2017 2017
Cerebral Infarction, Left Hemisphere
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 1.000 1 2002 2002
Cerebral Infarction, Right Hemisphere
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 1.000 1 2002 2002
Anterior Choroidal Artery Infarction
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 1.000 1 2002 2002
Posterior Choroidal Artery Infarction
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 1.000 1 2002 2002
CUI: C0751230
Disease: Hypothalamic Dysfunction Syndromes
Hypothalamic Dysfunction Syndromes
disease Nervous System Diseases Disease or Syndrome 12 0.010 None 1.000 1 2014 2014
CUI: C0751014
Disease: Subcortical Infarction
Subcortical Infarction
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 13 0.300 None 1.000 1 2002 2002
CUI: C2362914
Disease: clinical depression
clinical depression
disease Mental Disorders Mental or Behavioral Dysfunction 14 0.300 None 1.000 1 1992 1992
CUI: C1839130
Disease: Dystonia 3, Torsion, X-Linked
Dystonia 3, Torsion, X-Linked
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 15 1 0.010 None 1.000 1 2013 2013
CUI: C0042420
Disease: Vasovagal syncope
Vasovagal syncope
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 16 1 0.010 None 1.000 1 2017 2017
CUI: C1836438
Disease: Familial neurocardiogenic syncope
Familial neurocardiogenic syncope
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 16 1 0.010 None 1.000 1 2017 2017
CUI: C0020564
Disease: Hypertrophy
Hypertrophy
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 18 0.300 None 1.000 1 1997 1997
CUI: C0001957
Disease: Alcohol Withdrawal Delirium
Alcohol Withdrawal Delirium
disease Nervous System Diseases; Chemically-Induced Disorders; Mental Disorders Disease or Syndrome 23 8 0.010 None 1.000 1 2001 2001
CUI: C0014558
Disease: Uncinate Epilepsy
Uncinate Epilepsy
disease Nervous System Diseases Disease or Syndrome 23 0.300 None 1.000 1 2005 2005
CUI: C0085625
Disease: Hypoalgesia
Hypoalgesia
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Sign or Symptom 23 7 0.010 None 1.000 1 2003 2003
Epilepsy, Benign Psychomotor, Childhood
disease Nervous System Diseases Disease or Syndrome 23 0.300 None 1.000 1 2005 2005
CUI: C0151564
Disease: Cogwheel Rigidity
Cogwheel Rigidity
phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases Sign or Symptom 24 1 0.300 None 1.000 1 2000 2000
Superficial spreading malignant melanoma of skin
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 25 2 0.010 None 1.000 1 2017 2017
CUI: C4048305
Disease: Neuroepithelioma
Neuroepithelioma
disease Neoplastic Process 28 0.020 None 1.000 2 1990 2001
CUI: C0001818
Disease: Agoraphobia
Agoraphobia
disease Mental Disorders Mental or Behavioral Dysfunction 29 11 0.010 None 1.000 1 2008 2008
CUI: C0393682
Disease: Epilepsy, Lateral Temporal
Epilepsy, Lateral Temporal
disease Nervous System Diseases Disease or Syndrome 29 1 0.300 None 1.000 1 2005 2005
CUI: C0342543
Disease: Central Precocious Puberty
Central Precocious Puberty
disease Endocrine System Diseases Disease or Syndrome 32 2 0.020 None 1.000 2 2017 2017
CUI: C0221292
Disease: Basophilic leukemia
Basophilic leukemia
disease Neoplasms Neoplastic Process 32 3 0.010 None 1.000 1 2018 2018
CUI: C0751217
Disease: Hyperkinesia, Generalized
Hyperkinesia, Generalized
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 32 0.300 None 1.000 1 2009 2009