CALB2, calbindin 2, 794

N. diseases: 124; N. variants: 1
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: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 4081 1204 0.020 None 1.000 2 2015 2017
CUI: C0334513
Disease: Sarcomatoid Mesothelioma
Sarcomatoid Mesothelioma
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 10 0.020 None 1.000 2 2007 2017
CUI: C3838965
Disease: Microcystic stromal tumor
Microcystic stromal tumor
disease Neoplastic Process 8 2 0.020 None 1.000 2 2018 2019
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
Complete Trisomy 21 Syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 669 77 0.020 None 1.000 2 2016 2018
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
disease Digestive System Diseases; Neoplasms Neoplastic Process 2969 688 0.020 None 1.000 2 2008 2010
CUI: C0014544
Disease: Epilepsy
Epilepsy
disease Nervous System Diseases Disease or Syndrome 1215 339 0.020 None 1.000 2 2017 2017
CUI: C0013080
Disease: Down Syndrome
Down Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 766 80 0.020 None 1.000 2 2016 2018
Malignant Mesothelioma of Peritoneum
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 65 2 0.020 None 1.000 2 2006 2016
CUI: C0002448
Disease: Ameloblastoma
Ameloblastoma
disease Neoplasms Neoplastic Process 174 4 0.020 None 1.000 2 2008 2008
CUI: C0039747
Disease: Thecoma
Thecoma
disease Neoplasms Neoplastic Process 8 0.010 None 1.000 1 2018 2018
CUI: C0457536
Disease: Peripheral ameloblastoma
Peripheral ameloblastoma
disease Neoplasms Neoplastic Process 2 0.010 None 1.000 1 2018 2018
CUI: C0345992
Disease: Pilar tumor
Pilar tumor
disease Neoplasms Neoplastic Process 3 0.010 None 1.000 1 2019 2019
Sialic Acid Storage Disease, Finnish Type (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 47 44 0.010 None 1.000 1 2018 2018
CUI: C0862312
Disease: Epithelioid mesothelioma, malignant
Epithelioid mesothelioma, malignant
disease Neoplasms Neoplastic Process 32 0.010 None 1.000 1 2016 2016
CUI: C0349658
Disease: Trichoepithelioma
Trichoepithelioma
disease Neoplasms Neoplastic Process 24 3 0.010 None 1.000 1 2019 2019
CUI: C0751213
Disease: Tactile Allodynia
Tactile Allodynia
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 114 0.010 None 1.000 1 2019 2019
CUI: C0401149
Disease: Chronic constipation
Chronic constipation
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 47 16 0.010 None 1.000 1 2016 2016
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Mental or Behavioral Dysfunction 1263 112 0.010 None 1.000 1 2020 2020
CUI: C0474808
Disease: Follicular neoplasm
Follicular neoplasm
disease Neoplasms Neoplastic Process 68 5 0.010 None 1.000 1 2019 2019
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 6776 2793 0.010 None 1.000 1 2017 2017
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder
group Mental Disorders Mental or Behavioral Dysfunction 328 49 0.010 None 1.000 1 2017 2017
Short segment Hirschsprung's disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 5 1 0.010 None 1.000 1 2016 2016
CUI: C1258666
Disease: Myxoid cyst
Myxoid cyst
disease Neoplasms; Skin and Connective Tissue Diseases Disease or Syndrome 106 0.010 None 1.000 1 2019 2019
CUI: C1865349
Disease: Ethylmalonic encephalopathy
Ethylmalonic encephalopathy
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 26 33 0.010 None 1.000 1 2017 2017
CUI: C1960546
Disease: Myxoma of heart
Myxoma of heart
disease Neoplasms; Cardiovascular Diseases Neoplastic Process 23 0.010 None 1.000 1 2001 2001