TNFRSF1A, TNF receptor superfamily member 1A, 7132

N. diseases: 487; N. variants: 48
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: C0342611
Disease: Familial non-neuropathic amyloidosis
Familial non-neuropathic amyloidosis 		disease Nutritional and Metabolic Diseases Disease or Syndrome 2 0.200 None 1.000 2 1998 2010
CUI: C1719313
Disease: Hereditary amyloid nephropathy
Hereditary amyloid nephropathy 		disease Disease or Syndrome 2 0.200 None 1.000 2 1998 2010
CUI: C0149910
Disease: Intermittent joint effusion
Intermittent joint effusion 		disease Musculoskeletal Diseases Disease or Syndrome 2 0.300 None 1.000 1 2013 2013
CUI: C0155679
Disease: Acute pericarditis
Acute pericarditis 		disease Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2013 2013
CUI: C0847014
Disease: fever with rash
fever with rash 		phenotype Sign or Symptom 2 0.010 None 1.000 1 2012 2012
CUI: C4707791
Disease: Inflammatory myopathy with abundant macrophages
Inflammatory myopathy with abundant macrophages 		disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 2 0.010 None 1.000 1 2014 2014
CUI: C4707790
Disease: Idiopathic recurrent pericarditis
Idiopathic recurrent pericarditis 		disease Cardiovascular Diseases Disease or Syndrome 3 0.020 None 1.000 2 2010 2010
CUI: C3151062
Disease: INFECTIONS, RECURRENT, WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, AND CARDIOVASCULAR MALFORMATIONS
INFECTIONS, RECURRENT, WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, AND CARDIOVASCULAR MALFORMATIONS 		disease Disease or Syndrome 3 1 0.010 None 1.000 1 2019 2019
CUI: C1761613
Disease: Conjunctival hyperemia
Conjunctival hyperemia 		phenotype Eye Diseases Finding 3 0.100 None 0
CUI: C0032308
Disease: Staphylococcal Pneumonia
Staphylococcal Pneumonia 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 4 0.010 None 1.000 1 2012 2012
CUI: C0152965
Disease: Staphylococcal sepsis
Staphylococcal sepsis 		disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 4 0.010 None 1.000 1 2018 2018
CUI: C0015645
Disease: Fasciitis
Fasciitis 		disease Musculoskeletal Diseases Disease or Syndrome 4 0.100 None 0
CUI: C0262621
Disease: Abnormality of the sacroiliac joint
Abnormality of the sacroiliac joint 		phenotype Finding 4 0.100 None 0
CUI: C0267839
Disease: Hepatic amyloidosis
Hepatic amyloidosis 		disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 4 0.100 None 0
CUI: C0333998
Disease: Nodular lymphoid hyperplasia
Nodular lymphoid hyperplasia 		disease Disease or Syndrome 5 0.010 None 1.000 1 2019 2019
CUI: C4268691
Disease: Tumor necrosis factor receptor associated periodic syndrome [TRAPS]
Tumor necrosis factor receptor associated periodic syndrome [TRAPS] 		disease Disease or Syndrome 6 2 0.100 None 1.000 20 2 2000 2019
CUI: C0585274
Disease: Periodic syndrome
Periodic syndrome 		disease Disease or Syndrome 6 0.080 None 1.000 8 2000 2016
CUI: C0007177
Disease: Cardiac Tamponade
Cardiac Tamponade 		disease Cardiovascular Diseases Disease or Syndrome 8 1 0.010 None 1.000 1 1 2017 2017
CUI: C0019114
Disease: Hemosiderosis
Hemosiderosis 		disease Nutritional and Metabolic Diseases Disease or Syndrome 8 2 0.010 None 1.000 1 2017 2017
CUI: C1404931
Disease: Septic peritonitis
Septic peritonitis 		disease Disease or Syndrome 8 0.010 None 1.000 1 2019 2019
CUI: C0747556
Disease: Recurrent pharyngitis
Recurrent pharyngitis 		phenotype Infections; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Sign or Symptom 8 0.100 None 0
CUI: C0001416
Disease: Adenitis
Adenitis 		phenotype Hemic and Lymphatic Diseases Sign or Symptom 9 1 0.010 None 1.000 1 1 2011 2011
CUI: C0745754
Disease: Hepatic granuloma
Hepatic granuloma 		disease Digestive System Diseases Disease or Syndrome 9 0.010 None 1.000 1 2019 2019
CUI: C1527396
Disease: Fibrocystic Disease of Pancreas
Fibrocystic Disease of Pancreas 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases Disease or Syndrome 9 0.300 None 1.000 1 2006 2006
CUI: C0042166
Disease: Uveitis, Intermediate
Uveitis, Intermediate 		disease Eye Diseases Disease or Syndrome 10 10 0.010 None 1.000 1 2013 2013