SERPINB6, serpin family B member 6, 5269

N. diseases: 128; 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: C3150704
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 91
DEAFNESS, AUTOSOMAL RECESSIVE 91 		disease Disease or Syndrome 1 1 0.600 strong 1.000 1 1 1995 1995
CUI: C0024901
Disease: Mastocytosis, Diffuse Cutaneous
Mastocytosis, Diffuse Cutaneous 		disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 4 0.010 None 1.000 1 2004 2004
CUI: C0949570
Disease: Wheat Hypersensitivity
Wheat Hypersensitivity 		disease Immune System Diseases Disease or Syndrome 11 2 0.010 None 1.000 1 2009 2009
CUI: C1842138
Disease: Progressive hearing impairment
Progressive hearing impairment 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Finding 14 2 0.100 None 0
CUI: C1142536
Disease: Pneumonia due to methicillin resistant Staphylococcus aureus
Pneumonia due to methicillin resistant Staphylococcus aureus 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 15 0.010 None 1.000 1 2015 2015
CUI: C0740919
Disease: Allergy to grass pollen
Allergy to grass pollen 		disease Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 17 0.010 None 1.000 1 2011 2011
CUI: C1868594
Disease: Perry Syndrome
Perry Syndrome 		disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Behavior and Behavior Mechanisms Disease or Syndrome 19 9 0.020 None 1.000 2 2009 2010
CUI: C1443237
Disease: Healthcare associated pneumonia
Healthcare associated pneumonia 		phenotype Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases Disease or Syndrome 22 2 0.010 None 1.000 1 2017 2017
CUI: C3280586
Disease: Mannose-Binding Protein Deficiency
Mannose-Binding Protein Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 25 3 0.010 None < 0.001 1 2013 2013
CUI: C0024897
Disease: Mastocytoma
Mastocytoma 		disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 26 4 0.010 None 1.000 1 2004 2004
CUI: C2242987
Disease: Benign Mastocytoma
Benign Mastocytoma 		disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 26 4 0.010 None 1.000 1 2004 2004
CUI: C0312414
Disease: Menstrual spotting
Menstrual spotting 		phenotype Sign or Symptom 27 2 0.010 None 1.000 1 2017 2017
CUI: C1827301
Disease: Extensively Drug-Resistant Tuberculosis
Extensively Drug-Resistant Tuberculosis 		phenotype Infections Disease or Syndrome 29 0.010 None 1.000 1 2016 2016
CUI: C3669246
Disease: Mammary adenocarcinoma
Mammary adenocarcinoma 		disease Neoplastic Process 29 0.010 None 1.000 1 2004 2004
CUI: C0007125
Disease: Carcinoma, Ehrlich Tumor
Carcinoma, Ehrlich Tumor 		disease Neoplasms Neoplastic Process; Experimental Model of Disease 30 0.010 None 1.000 1 2018 2018
CUI: C0276680
Disease: Infection by Candida albicans
Infection by Candida albicans 		disease Infections Disease or Syndrome 30 0.010 None 1.000 1 2004 2004
CUI: C0014009
Disease: Empyema
Empyema 		disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 31 0.010 None 1.000 1 2013 2013
CUI: C0334664
Disease: Mast Cell Neoplasm
Mast Cell Neoplasm 		disease Neoplasms Neoplastic Process 33 4 0.010 None 1.000 1 2004 2004
CUI: C0271994
Disease: Hereditary persistence of fetal hemoglobin thalassemia
Hereditary persistence of fetal hemoglobin thalassemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 35 0.010 None 1.000 1 1993 1993
CUI: C0339901
Disease: Acute respiratory infections
Acute respiratory infections 		group Infections; Respiratory Tract Diseases Disease or Syndrome 35 0.010 None 1.000 1 2012 2012
CUI: C0472767
Disease: Beta thalassemia intermedia
Beta thalassemia intermedia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 37 12 0.010 None 1.000 1 2016 2016
CUI: C0266815
Disease: Cow milk allergy
Cow milk allergy 		phenotype Digestive System Diseases; Immune System Diseases Disease or Syndrome 38 0.010 None 1.000 1 2019 2019
CUI: C0581381
Disease: Recurrent upper respiratory tract infection
Recurrent upper respiratory tract infection 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 52 3 0.010 None 1.000 1 2012 2012
CUI: C1320214
Disease: Invasive Streptococcus pneumoniae disease
Invasive Streptococcus pneumoniae disease 		disease Infections Disease or Syndrome 55 9 0.020 None 1.000 2 2013 2019
CUI: C0234233
Disease: Sore to touch
Sore to touch 		phenotype Pathological Conditions, Signs and Symptoms; Mental Disorders Sign or Symptom 56 8 0.010 None 1.000 1 2019 2019