MAOB, monoamine oxidase B, 4129

N. diseases: 152; N. variants: 8
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.
Aromatic amino acid decarboxylase deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 5 7 0.010 None 1.000 1 2016 2016
Deficiency of aromatic-L-amino-acid decarboxylase
disease Disease or Syndrome 7 16 0.010 None 1.000 1 2016 2016
CUI: C0334419
Disease: Pheochromocytoma, malignant
Pheochromocytoma, malignant
disease Neoplasms; Endocrine System Diseases Neoplastic Process 11 1 0.010 None 1.000 1 2010 2010
CUI: C0033893
Disease: Tension Headache
Tension Headache
disease Nervous System Diseases Disease or Syndrome 12 6 0.010 None 1.000 1 2015 2015
CUI: C0393574
Disease: Huntington Disease, Late Onset
Huntington Disease, Late Onset
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders Disease or Syndrome 12 0.300 None 1.000 1 2011 2011
Akinetic-Rigid Variant of Huntington Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders Disease or Syndrome 12 0.300 None 1.000 1 2011 2011
CUI: C0751208
Disease: Juvenile Huntington Disease
Juvenile Huntington Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders Disease or Syndrome 12 0.300 None 1.000 1 2011 2011
Fulminant Hepatic Failure with Cerebral Edema
disease Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 13 0.300 None 1.000 1 1999 1999
CUI: C0751198
Disease: Hepatic Stupor
Hepatic Stupor
disease Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 13 0.300 None 1.000 1 1999 1999
CUI: C0019147
Disease: Hepatic Coma
Hepatic Coma
disease Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 14 0.300 None 1.000 1 1999 1999
CUI: C0005122
Disease: Beriberi
Beriberi
disease Nutritional and Metabolic Diseases Disease or Syndrome 16 0.010 None 1.000 1 2017 2017
CUI: C2220255
Disease: Motor disturbances
Motor disturbances
phenotype Sign or Symptom 16 1 0.010 None 1.000 1 2004 2004
CUI: C0039841
Disease: Thiamine Deficiency
Thiamine Deficiency
disease Nutritional and Metabolic Diseases Disease or Syndrome 17 0.010 None 1.000 1 2017 2017
CUI: C0522174
Disease: Delinquent behavior
Delinquent behavior
phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 17 2 0.010 None 1.000 1 2016 2016
CUI: C0392702
Disease: Abnormal involuntary movement
Abnormal involuntary movement
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 22 10 0.010 None 1.000 1 2004 2004
CUI: C0236848
Disease: Age-related cognitive decline
Age-related cognitive decline
disease Mental Disorders Mental or Behavioral Dysfunction 24 3 0.010 None 1.000 1 2018 2018
CUI: C0002888
Disease: Anemia, Megaloblastic
Anemia, Megaloblastic
disease Hemic and Lymphatic Diseases Disease or Syndrome 26 2 0.300 None 1.000 1 1980 1980
CUI: C0030662
Disease: Gambling, Pathological
Gambling, Pathological
disease Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 26 9 0.010 None 1.000 1 2000 2000
CUI: C0029121
Disease: Oppositional Defiant Disorder
Oppositional Defiant Disorder
disease Mental Disorders Mental or Behavioral Dysfunction 27 9 0.010 None 1.000 1 2008 2008
CUI: C0149654
Disease: Conduct Disorder
Conduct Disorder
disease Mental Disorders Mental or Behavioral Dysfunction 34 18 0.010 None < 0.001 1 1 2016 2016
CUI: C1257877
Disease: Pheochromocytoma, Extra-Adrenal
Pheochromocytoma, Extra-Adrenal
disease Neoplasms Neoplastic Process 38 5 0.300 None 1.000 1 2012 2012
CUI: C0751434
Disease: Classical phenylketonuria
Classical phenylketonuria
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 42 385 0.010 None 1.000 1 2004 2004
CUI: C0020514
Disease: Hyperprolactinemia
Hyperprolactinemia
disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 48 10 0.010 None 1.000 1 1 2019 2019
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease
disease Nervous System Diseases Disease or Syndrome 51 32 0.010 None 1.000 1 2007 2007
CUI: C0564567
Disease: Impulsive character (finding)
Impulsive character (finding)
phenotype Mental or Behavioral Dysfunction 52 19 0.010 None 1.000 1 2016 2016