SORBS1, sorbin and SH3 domain containing 1, 10580

N. diseases: 124; N. variants: 28
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: C0086942
Disease: Rous Sarcoma
Rous Sarcoma
disease Neoplasms; Infections; Animal Diseases Neoplastic Process; Experimental Model of Disease 60 0.010 None 1.000 1 1990 1990
CUI: C0280474
Disease: Childhood Glioblastoma
Childhood Glioblastoma
disease Neoplasms Neoplastic Process 2527 98 0.010 None 1.000 1 2017 2017
CUI: C0312414
Disease: Menstrual spotting
Menstrual spotting
phenotype Sign or Symptom 27 2 0.010 None 1.000 1 2017 2017
CUI: C0333559
Disease: Infarction, Lacunar
Infarction, Lacunar
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 36 18 0.010 None 1.000 1 1 2008 2008
Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 296 9 0.010 None 1.000 1 2018 2018
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: C0342541
Disease: Precocious pubarche
Precocious pubarche
disease Endocrine System Diseases Disease or Syndrome 30 11 0.010 None < 0.001 1 1 2003 2003
MRSA - Methicillin resistant Staphylococcus aureus infection
disease Infections Disease or Syndrome 222 1 0.010 None 1.000 1 2015 2015
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
disease Neoplasms; Male Urogenital Diseases Neoplastic Process 4502 1082 0.010 None 1.000 1 2017 2017
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
disease Digestive System Diseases Disease or Syndrome 1058 222 0.010 None 1.000 1 2018 2018
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: C0476227
Disease: pricking of skin
pricking of skin
phenotype Sign or Symptom 65 1 0.010 None 1.000 1 2017 2017
Recurrent upper respiratory tract infection
disease Infections; Respiratory Tract Diseases Disease or Syndrome 52 3 0.010 None 1.000 1 2012 2012
CUI: C0280100
Disease: Solid Neoplasm
Solid Neoplasm
phenotype Neoplasms Neoplastic Process 1145 24 0.010 None 1.000 1 2018 2018
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
disease Neoplasms Neoplastic Process 2528 98 0.010 None 1.000 1 2017 2017
CUI: C0152244
Disease: Bone Cysts, Aneurysmal
Bone Cysts, Aneurysmal
disease Neoplasms; Musculoskeletal Diseases Disease or Syndrome 79 5 0.010 None 1.000 1 2016 2016
CUI: C0155862
Disease: Streptococcal pneumonia
Streptococcal pneumonia
disease Infections; Respiratory Tract Diseases Disease or Syndrome 100 2 0.010 None < 0.001 1 2017 2017
CUI: C0205969
Disease: Thymic Carcinoma
Thymic Carcinoma
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 82 8 0.010 None 1.000 1 2018 2018
CUI: C0206081
Disease: Hyperandrogenism
Hyperandrogenism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 108 24 0.010 None 1.000 1 1 2003 2003
CUI: C0206526
Disease: Tuberculosis, Multidrug-Resistant
Tuberculosis, Multidrug-Resistant
disease Infections Disease or Syndrome 67 8 0.010 None 1.000 1 5 2018 2018
CUI: C0237123
Disease: Alcohol or Other Drugs use
Alcohol or Other Drugs use
disease Mental or Behavioral Dysfunction 108 21 0.010 None 1.000 1 2020 2020
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 1179 64 0.010 None 1.000 1 2017 2017
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
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: C0275518
Disease: Acute infectious disease
Acute infectious disease
group Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 198 5 0.010 None 1.000 1 2010 2010