APP, amyloid beta precursor protein, 351

N. diseases: 485; N. variants: 114
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.
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1 5 0.700 None 1.000 7 5 1990 2010
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.300 None 1.000 2 1990 2000
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.300 None 1.000 2 1990 2000
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.300 None 1.000 2 1990 2000
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.300 None 1.000 2 1990 2000
Hereditary cerebrovascular amyloidosis
disease Congenital Abnormality 1 0.010 None 1.000 1 2009 2009
CUI: C0679441
Disease: Disorder of olfactory system
Disorder of olfactory system
group Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C0742115
Disease: Cerebritis
Cerebritis
disease Infections; Nervous System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C4025264
Disease: Recurrent cerebral hemorrhage
Recurrent cerebral hemorrhage
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.110 None 1.000 1 2004 2004
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT
phenotype Finding 1 1 0.100 None 0 1
CUI: C0600074
Disease: Autotomy
Autotomy
disease Mental or Behavioral Dysfunction 2 0.010 None 1.000 1 2010 2010
CUI: C1411876
Disease: Developmental arithmetic disorder
Developmental arithmetic disorder
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Mental or Behavioral Dysfunction 2 0.010 None 1.000 1 1993 1993
Primary angiitis of the central nervous system
disease Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C0149854
Disease: Cerebellar hemorrhage
Cerebellar hemorrhage
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 2 0.100 None 0
CUI: C1836791
Disease: Tortuous cerebral arteries
Tortuous cerebral arteries
phenotype Finding 2 1 0.100 None 0
CUI: C0241832
Disease: Cerebrovascular Insufficiency
Cerebrovascular Insufficiency
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 3 2 0.010 None 1.000 1 1 1999 1999
CUI: C2363813
Disease: Short-term memory impairment
Short-term memory impairment
disease Mental or Behavioral Dysfunction 3 0.010 None 1.000 1 2011 2011
CUI: C2931257
Disease: Alzheimer disease type 1
Alzheimer disease type 1
disease Nervous System Diseases; Mental Disorders Disease or Syndrome 3 10 0.100 None 0 10
CUI: C0520574
Disease: Cerebrovascular amyloidosis
Cerebrovascular amyloidosis
disease Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.030 None 1.000 3 1995 1999
CUI: C0749263
Disease: temporal pain
temporal pain
phenotype Disease or Syndrome 4 5 0.010 None 1.000 1 1 2013 2013
CUI: C1863052
Disease: ALZHEIMER DISEASE, FAMILIAL, 1
ALZHEIMER DISEASE, FAMILIAL, 1
disease Nervous System Diseases; Mental Disorders Disease or Syndrome 4 0.010 None 1.000 1 2002 2002
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q
disease Disease or Syndrome 4 3 0.010 None 1.000 1 2018 2018
CUI: C0268392
Disease: Localized amyloidosis
Localized amyloidosis
disease Nutritional and Metabolic Diseases Disease or Syndrome 5 0.010 None < 0.001 1 1999 1999
Sporadic Cerebral Amyloid Angiopathy
disease Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 6 0.310 None 1.000 2 2010 2011