APOA1, apolipoprotein A1, 335

N. diseases: 416; N. variants: 32
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.
APOLIPOPROTEIN A-I (MARBURG) PHENOTYPE
phenotype Finding 2 1 0.100 None 0 1
APOLIPOPROTEIN A-I (MILANO) PHENOTYPE
phenotype Finding 1 1 0.100 None 0 1
APOLIPOPROTEIN A-I (MUNSTER4) PHENOTYPE
phenotype Finding 1 1 0.100 None 0 1
CUI: C4551500
Disease: Amyloid Polyneuropathy, Iowa Type
Amyloid Polyneuropathy, Iowa Type
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 3 1 0.100 None 0 1
APOLIPOPROTEIN A-I (NORWAY) PHENOTYPE
phenotype Finding 2 1 0.100 None 0 1
Decreased HDL cholesterol concentration
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Finding 12 2 0.100 None 0
CUI: C1557375
Disease: Blurred Vision, CTCAE
Blurred Vision, CTCAE
phenotype Finding 26 0.100 None 0
APOLIPOPROTEIN A-I (GIESSEN) PHENOTYPE
phenotype Finding 1 1 0.100 None 0 1
APOLIPOPROTEIN A-I (MUNSTER3C) PHENOTYPE
phenotype Finding 2 1 0.100 None 0 1
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity
phenotype Eye Diseases Finding 113 5 0.100 None 0
CUI: C0043325
Disease: Xanthomatosis
Xanthomatosis
disease Nutritional and Metabolic Diseases Disease or Syndrome 20 10 0.100 None 0
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
phenotype Pathological Conditions, Signs and Symptoms Finding 345 19 0.100 None 0
APOLIPOPROTEIN A-I (MUNSTER3B) PHENOTYPE
phenotype Finding 2 1 0.100 None 0 1
APOLIPOPROTEIN A-I (BALTIMORE) PHENOTYPE
phenotype Finding 2 1 0.100 None 0 1
CUI: C4015843
Disease: AMYLOIDOSIS, CARDIAC AND CUTANEOUS
AMYLOIDOSIS, CARDIAC AND CUTANEOUS
disease Finding 2 2 0.100 None 0 2
CUI: C4521256
Disease: Glomerulopathy Assessment
Glomerulopathy Assessment
phenotype Diagnostic Procedure 84 0.300 limited 0
CUI: C0008370
Disease: Cholestasis
Cholestasis
disease Digestive System Diseases Disease or Syndrome 420 15 0.100 None 0
CUI: C0497156
Disease: Lymphadenopathy
Lymphadenopathy
phenotype Hemic and Lymphatic Diseases Disease or Syndrome 277 5 0.100 None 0
CUI: C0033687
Disease: Proteinuria
Proteinuria
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Finding 239 20 0.100 None 0
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal
phenotype Finding 130 12 0.100 None 0
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver
phenotype Finding 75 8 0.100 None 0
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Finding 523 30 0.100 None 0
CUI: C0375206
Disease: Hemiplegia/hemiparesis
Hemiplegia/hemiparesis
disease Disease or Syndrome 112 2 0.100 None 0
CUI: C0344232
Disease: Blurred vision
Blurred vision
phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Finding 28 2 0.100 None 0
CUI: C1862968
Disease: Generalized amyloid deposition
Generalized amyloid deposition
phenotype Nutritional and Metabolic Diseases Finding 6 0.100 None 0