Source: ALL

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
group 0.010 None 1.000 1 0 2013 2013
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
disease 0.010 None 1.000 1 0 2013 2013
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
group 0.010 None 1.000 1 0 2000 2000
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
group 0.010 None 1.000 1 0 2013 2013
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C0032914
Disease: Pre-Eclampsia
Pre-Eclampsia
phenotype 0.600 None 1.000 1 0 2012 2012
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C0033626
Disease: Protein Deficiency
Protein Deficiency
disease 0.010 None 1.000 1 0 2014 2014
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease
disease 0.010 None 1.000 1 0 2016 2016
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C1306893
Disease: Anomaly of placenta
Anomaly of placenta
phenotype 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision
disease 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
group 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C1840374
Disease: Elevated systolic blood pressure
Elevated systolic blood pressure
phenotype 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C1840375
Disease: Elevated diastolic blood pressure
Elevated diastolic blood pressure
phenotype 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
Abnormality of the hepatic vasculature
phenotype 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase
phenotype 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C2609414
Disease: Acute kidney injury
Acute kidney injury
disease 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C0851578
Disease: Sleep Disorders
Sleep Disorders
group 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
Diabetes Mellitus, Insulin-Dependent
disease 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C0018681
Disease: Headache
Headache
phenotype 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
phenotype 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
disease 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C0033687
Disease: Proteinuria
Proteinuria
phenotype 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C0037317
Disease: Sleep disturbances
Sleep disturbances
phenotype 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia
phenotype 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
CUI: C0231254
Disease: Increased body mass index
Increased body mass index
phenotype 0.100 None 0 0
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
corin, serine peptidase 0.695 0.538 6.5E-35
Small for gestational age (disorder)
phenotype 0.100 None 0 0