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.
CUI: C0339882
Disease: Laryngeal amyloidosis
Laryngeal amyloidosis 		disease Respiratory Tract Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 1 0.010 None 1.000 1 2009 2009
CUI: C2711472
Disease: Infection by Trypanosoma brucei brucei
Infection by Trypanosoma brucei brucei 		disease Infections Disease or Syndrome 1 0.010 None 1.000 1 1992 1992
CUI: C2880381
Disease: Arcus senilis, bilateral
Arcus senilis, bilateral 		disease Eye Diseases Disease or Syndrome 1 0.010 None 1.000 1 1991 1991
CUI: C4015830
Disease: APOLIPOPROTEIN A-I (MILANO) PHENOTYPE
APOLIPOPROTEIN A-I (MILANO) PHENOTYPE 		phenotype Finding 1 1 0.100 None 0 1
CUI: C4015832
Disease: APOLIPOPROTEIN A-I (MUNSTER4) PHENOTYPE
APOLIPOPROTEIN A-I (MUNSTER4) PHENOTYPE 		phenotype Finding 1 1 0.100 None 0 1
CUI: C4015833
Disease: APOLIPOPROTEIN A-I (GIESSEN) PHENOTYPE
APOLIPOPROTEIN A-I (GIESSEN) PHENOTYPE 		phenotype Finding 1 1 0.100 None 0 1
CUI: C0342898
Disease: Apolipoprotein A-I deficiency
Apolipoprotein A-I deficiency 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Pathologic Function 2 0.300 None 1.000 2 1993 1994
CUI: C3165209
Disease: High density lipoprotein deficiency
High density lipoprotein deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 2 0.020 None 1.000 2 1991 2009
CUI: C0079221
Disease: Determination of Death
Determination of Death 		phenotype Pathological Conditions, Signs and Symptoms Diagnostic Procedure 2 0.300 None 1.000 1 2011 2011
CUI: C0376297
Disease: Cardiac Death
Cardiac Death 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 2 0.300 None 1.000 1 2011 2011
CUI: C0544840
Disease: Nodular amyloidosis
Nodular amyloidosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Neoplastic Process 2 0.010 None 1.000 1 2012 2012
CUI: C1719315
Disease: Hereditary cardiac amyloidosis
Hereditary cardiac amyloidosis 		disease Disease or Syndrome 2 1 0.010 None 1.000 1 1999 1999
CUI: C4015831
Disease: APOLIPOPROTEIN A-I (MARBURG) PHENOTYPE
APOLIPOPROTEIN A-I (MARBURG) PHENOTYPE 		phenotype Finding 2 1 0.100 None 0 1
CUI: C4015834
Disease: APOLIPOPROTEIN A-I (MUNSTER3C) PHENOTYPE
APOLIPOPROTEIN A-I (MUNSTER3C) PHENOTYPE 		phenotype Finding 2 1 0.100 None 0 1
CUI: C4015835
Disease: APOLIPOPROTEIN A-I (MUNSTER3B) PHENOTYPE
APOLIPOPROTEIN A-I (MUNSTER3B) PHENOTYPE 		phenotype Finding 2 1 0.100 None 0 1
CUI: C4015839
Disease: APOLIPOPROTEIN A-I (BALTIMORE) PHENOTYPE
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: C4017713
Disease: APOLIPOPROTEIN A-I (NORWAY) PHENOTYPE
APOLIPOPROTEIN A-I (NORWAY) PHENOTYPE 		phenotype Finding 2 1 0.100 None 0 1
CUI: C0162279
Disease: Choroidal detachment
Choroidal detachment 		disease Eye Diseases Acquired Abnormality 3 0.010 None 1.000 1 2018 2018
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
CUI: C0267839
Disease: Hepatic amyloidosis
Hepatic amyloidosis 		disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 4 0.010 None 1.000 1 2003 2003
CUI: C4521075
Disease: Childhood Overweight
Childhood Overweight 		phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Finding 4 0.300 None 1.000 1 2014 2014
CUI: C4704955
Disease: Infant Overweight
Infant Overweight 		phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Finding 4 0.300 None 1.000 1 2014 2014
CUI: C4704956
Disease: Adolescent Overweight
Adolescent Overweight 		phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Finding 4 0.300 None 1.000 1 2014 2014
CUI: C0268392
Disease: Localized amyloidosis
Localized amyloidosis 		disease Nutritional and Metabolic Diseases Disease or Syndrome 5 0.010 None 1.000 1 2011 2011