SERPINA1, serpin family A member 1, 5265

N. diseases: 482; N. variants: 61
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: C3273033
Disease: Well Differentiated Hepatocellular Carcinoma
Well Differentiated Hepatocellular Carcinoma 		disease Digestive System Diseases; Neoplasms Neoplastic Process 8 0.010 None 1.000 1 1987 1987
CUI: C0264220
Disease: Chronic disease of respiratory system
Chronic disease of respiratory system 		group Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Disease or Syndrome 9 0.010 None 1.000 1 1993 1993
CUI: C0334357
Disease: Papillary cystic tumor
Papillary cystic tumor 		disease Neoplasms Neoplastic Process 9 0.010 None 1.000 1 1992 1992
CUI: C0027333
Disease: Nagana
Nagana 		disease Infections Disease or Syndrome 10 0.010 None 1.000 1 2019 2019
CUI: C0340613
Disease: Arterial aneurysm
Arterial aneurysm 		disease Cardiovascular Diseases Anatomical Abnormality 10 2 0.010 None 1.000 1 1996 1996
CUI: C1282975
Disease: von Willebrand Disease, Type 2N
von Willebrand Disease, Type 2N 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 10 11 0.010 None 1.000 1 2019 2019
CUI: C3544266
Disease: Hepatobiliary cancer
Hepatobiliary cancer 		disease Neoplastic Process 11 1 0.010 None 1.000 1 1992 1992
CUI: C0751157
Disease: FRAXE Syndrome
FRAXE Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 11 2 0.100 None 0 1
CUI: C0264393
Disease: Panacinar Emphysema
Panacinar Emphysema 		disease Respiratory Tract Diseases Disease or Syndrome 12 1 0.350 None 1.000 6 1981 2013
CUI: C0012817
Disease: Diverticulum
Diverticulum 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Anatomical Abnormality 12 0.010 None 1.000 1 2019 2019
CUI: C0042140
Disease: Uterine Prolapse
Uterine Prolapse 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Anatomical Abnormality 12 0.010 None 1.000 1 2012 2012
CUI: C0155870
Disease: Pneumonia and influenza
Pneumonia and influenza 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 12 2 0.010 None 1.000 1 2019 2019
CUI: C0206307
Disease: Canavan Disease
Canavan Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 12 65 0.010 None 1.000 1 2008 2008
CUI: C2350878
Disease: Focal Emphysema
Focal Emphysema 		disease Respiratory Tract Diseases Disease or Syndrome 12 0.300 None 1.000 1 1986 1986
CUI: C0035012
Disease: Reiter Syndrome
Reiter Syndrome 		disease Infections; Musculoskeletal Diseases Disease or Syndrome 14 0.020 None 1.000 2 1986 1987
CUI: C0221227
Disease: Centriacinar Emphysema
Centriacinar Emphysema 		disease Respiratory Tract Diseases Disease or Syndrome 14 3 0.300 None 1.000 1 1986 1986
CUI: C0267792
Disease: Hepatobiliary disease
Hepatobiliary disease 		disease Digestive System Diseases Disease or Syndrome 14 0.010 None 1.000 1 1976 1976
CUI: C0333440
Disease: Hyaline body
Hyaline body 		disease Anatomical Abnormality 14 0.010 None 1.000 1 2013 2013
CUI: C2930617
Disease: Pulmonary Fibrosis - from Asbestos Exposure
Pulmonary Fibrosis - from Asbestos Exposure 		disease Respiratory Tract Diseases; Occupational Diseases Disease or Syndrome 14 0.300 None 1.000 1 2002 2002
CUI: C4020848
Disease: Aneurysmal disease
Aneurysmal disease 		disease Disease or Syndrome 14 0.010 None 1.000 1 1996 1996
CUI: C0010201
Disease: Chronic cough
Chronic cough 		phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Sign or Symptom 14 1 0.100 None 0 1
CUI: C0267809
Disease: Cirrhosis, Cryptogenic
Cirrhosis, Cryptogenic 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 15 5 0.020 None 1.000 2 1981 1983
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 2018 2018
CUI: C0302280
Disease: Adrenogenital Syndrome
Adrenogenital Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 16 0.010 None 1.000 1 2019 2019
CUI: C0425782
Disease: Breast size
Breast size 		phenotype Finding 16 38 0.100 None 1.000 1 1 2016 2016