SAA1, serum amyloid A1, 6288

N. diseases: 188; N. variants: 6
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: C0264964
Disease: Aneurysm of popliteal artery
Aneurysm of popliteal artery
disease Disease or Syndrome 2 0.010 None 1.000 1 2020 2020
CUI: C2939462
Disease: Immunoglobulin deposition disease
Immunoglobulin deposition disease
disease Neoplasms Neoplastic Process 5 1 0.010 None 1.000 1 1986 1986
CUI: C3888004
Disease: HERMANSKY-PUDLAK SYNDROME 5
HERMANSKY-PUDLAK SYNDROME 5
disease Disease or Syndrome 6 20 0.010 None 1.000 1 2010 2010
CUI: C4023170
Disease: Abnormal oral mucosa morphology
Abnormal oral mucosa morphology
disease Anatomical Abnormality 6 0.100 None 0
CUI: C1135188
Disease: Critical illness myopathy
Critical illness myopathy
disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 8 0.010 None 1.000 1 2014 2014
CUI: C3273010
Disease: Inflammatory Hepatocellular Adenoma
Inflammatory Hepatocellular Adenoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 10 0.010 None 1.000 1 2015 2015
CUI: C0398691
Disease: Hyperimmunoglobulinemia D
Hyperimmunoglobulinemia D
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 12 33 0.010 None 1.000 1 2005 2005
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
Amyloid Neuropathies, Familial
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 15 16 0.010 None 1.000 1 1984 1984
CUI: C0030196
Disease: Pain in limb
Pain in limb
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 16 5 0.010 None 1.000 1 2017 2017
CUI: C0151594
Disease: Hemorrhagic diarrhea
Hemorrhagic diarrhea
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 16 0.010 None < 0.001 1 2004 2004
CUI: C0268382
Disease: Amyloid nephropathy
Amyloid nephropathy
disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 20 7 0.140 None 0.750 4 2000 2009
CUI: C0342731
Disease: Deficiency of mevalonate kinase
Deficiency of mevalonate kinase
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 20 23 0.010 None 1.000 1 2005 2005
CUI: C0268380
Disease: Systemic amyloidosis
Systemic amyloidosis
disease Nutritional and Metabolic Diseases Disease or Syndrome 21 10 0.010 None 1.000 1 1986 1986
CUI: C0281479
Disease: Primary Systemic Amyloidosis
Primary Systemic Amyloidosis
disease Neoplasms; Nutritional and Metabolic Diseases; Immune System Diseases Neoplastic Process 27 10 0.010 None 1.000 1 1986 1986
CUI: C0542518
Disease: Enlarged kidney
Enlarged kidney
phenotype Finding 27 2 0.100 None 0
CUI: C1290807
Disease: Diarrheal disorder
Diarrheal disorder
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 32 0.010 None 1.000 1 2003 2003
Intestinal infectious disease (disorder)
group Digestive System Diseases; Infections Disease or Syndrome 34 0.010 None 1.000 1 2017 2017
CUI: C0036983
Disease: Septic Shock
Septic Shock
phenotype Pathological Conditions, Signs and Symptoms; Infections Pathologic Function 37 1 0.010 None 1.000 1 2008 2008
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
disease Nutritional and Metabolic Diseases Disease or Syndrome 38 10 0.100 None 0.931 29 1986 2018
Cryopyrin-Associated Periodic Syndromes
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 39 12 0.010 None 1.000 1 2008 2008
CUI: C0221014
Disease: Reactive systemic amyloidosis
Reactive systemic amyloidosis
disease Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 41 11 0.400 None 0.935 31 1986 2018
CUI: C0003865
Disease: Arthritis, Adjuvant-Induced
Arthritis, Adjuvant-Induced
disease Musculoskeletal Diseases Experimental Model of Disease 43 0.300 None 1.000 1 2005 2005
CUI: C0085693
Disease: Acute appendicitis NOS (disorder)
Acute appendicitis NOS (disorder)
disease Digestive System Diseases; Infections Disease or Syndrome 43 2 0.010 None 1.000 1 2019 2019
CUI: C0971858
Disease: Arthritis, Collagen-Induced
Arthritis, Collagen-Induced
disease Musculoskeletal Diseases Experimental Model of Disease 43 0.300 None 1.000 1 2005 2005
CUI: C0993582
Disease: Arthritis, Experimental
Arthritis, Experimental
disease Musculoskeletal Diseases Experimental Model of Disease 43 0.300 None 1.000 1 2005 2005