SAA1, serum amyloid A1, 6288

N. diseases: 82; N. variants: 3
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: C0221014
Disease: Reactive systemic amyloidosis
Reactive systemic amyloidosis 		disease Disease or Syndrome 26 5 0.400 0.875 24 1 1986 2015
CUI: C0971858
Disease: Arthritis, Collagen-Induced
Arthritis, Collagen-Induced 		disease Musculoskeletal Diseases Experimental Model of Disease 43 0.300 1 2005 2005
CUI: C0011616
Disease: Contact Dermatitis
Contact Dermatitis 		disease Skin and Connective Tissue Diseases Disease or Syndrome 86 3 0.300 1 2005 2005
CUI: C0003865
Disease: Arthritis, Adjuvant-Induced
Arthritis, Adjuvant-Induced 		disease Musculoskeletal Diseases Experimental Model of Disease 43 0.300 1 2005 2005
CUI: C0993582
Disease: Arthritis, Experimental
Arthritis, Experimental 		disease Musculoskeletal Diseases Experimental Model of Disease 43 0.300 1 2005 2005
CUI: C0162351
Disease: Contact hypersensitivity
Contact hypersensitivity 		phenotype Skin and Connective Tissue Diseases Pathologic Function 71 0.300 1 2005 2005
CUI: C0268382
Disease: Amyloid nephropathy
Amyloid nephropathy 		disease Disease or Syndrome 20 4 0.150 0.800 5 2000 2010
CUI: C0002726
Disease: Amyloidosis
Amyloidosis 		disease Nutritional and Metabolic Diseases Disease or Syndrome 832 120 0.100 1.000 21 1985 2016
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		disease Immune System Diseases; Musculoskeletal Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 1832 1878 0.100 1.000 12 1986 2008
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		group Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 638 93 0.100 0
CUI: C0020649
Disease: Hypotension
Hypotension 		phenotype Cardiovascular Diseases Finding 88 0.100 0
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly 		phenotype Digestive System Diseases; Pathological Conditions, Signs and Symptoms Finding 372 0.100 0
CUI: C0033687
Disease: Proteinuria
Proteinuria 		phenotype Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Pathological Conditions, Signs and Symptoms Finding 183 5 0.100 0
CUI: C0748318
Disease: Progressive renal failure
Progressive renal failure 		phenotype Finding 20 3 0.100 0
CUI: C4023170
Disease: Abnormality of oral mucosa
Abnormality of oral mucosa 		phenotype Anatomical Abnormality 6 0.100 0
CUI: C0162429
Disease: Malnutrition
Malnutrition 		disease Nutritional and Metabolic Diseases Disease or Syndrome 224 16 0.100 0
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		phenotype Cardiovascular Diseases Pathologic Function 89 218 0.100 0
CUI: C0042963
Disease: Vomiting
Vomiting 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 186 14 0.100 0
CUI: C0687713
Disease: Gastrointestinal pain
Gastrointestinal pain 		phenotype Sign or Symptom 139 0.100 0
CUI: C0542518
Disease: Enlarged kidney
Enlarged kidney 		phenotype Finding 22 0.100 0
CUI: C0401151
Disease: Chronic diarrhea
Chronic diarrhea 		disease Disease or Syndrome 41 1 0.100 0
CUI: C0232487
Disease: Abdominal discomfort
Abdominal discomfort 		phenotype Sign or Symptom 137 0.100 0
CUI: C1408258
Disease: Kidney damage
Kidney damage 		phenotype Finding 46 2 0.100 0
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		group Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 379 120 0.100 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 152 2 0.100 0