UCN3, urocortin 3, 114131

N. diseases: 82; N. variants: 0
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: C4288141
Disease: TERT Deficiency
TERT Deficiency
disease Immune System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
Retinal microaneurysm with diabetes mellitus
disease Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C0014013
Disease: Empyema, Pleural
Empyema, Pleural
disease Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C3160792
Disease: Lamellar macular hole
Lamellar macular hole
disease Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
Mild non-proliferative diabetic retinopathy
disease Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome 6 0.010 None 1.000 1 2019 2019
CUI: C0020636
Disease: underdevelopment
underdevelopment
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 22 0.010 None 1.000 1 2019 2019
CUI: C0742038
Disease: Cerebellar signs
Cerebellar signs
phenotype Sign or Symptom 24 5 0.010 None 1.000 1 2019 2019
CUI: C0600142
Disease: Hot flushes
Hot flushes
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 32 1 0.010 None 1.000 1 2019 2019
CUI: C1262048
Disease: Glial scar
Glial scar
phenotype Acquired Abnormality 51 0.010 None 1.000 1 2019 2019
CUI: C0343804
Disease: Chronic Chagas' disease
Chronic Chagas' disease
disease Infections Disease or Syndrome 52 4 0.010 None 1.000 1 2018 2018
CUI: C0004626
Disease: Pneumonia, Bacterial
Pneumonia, Bacterial
group Infections; Respiratory Tract Diseases Disease or Syndrome 66 2 0.010 None 1.000 1 2019 2019
CUI: C0345958
Disease: Large cell carcinoma of lung
Large cell carcinoma of lung
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 67 7 0.010 None 1.000 1 2017 2017
CUI: C0410207
Disease: Tubular Aggregate Myopathy
Tubular Aggregate Myopathy
disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 67 5 0.010 None 1.000 1 2011 2011
CUI: C0037090
Disease: Signs and Symptoms, Respiratory
Signs and Symptoms, Respiratory
group Pathological Conditions, Signs and Symptoms Sign or Symptom 73 10 0.010 None 1.000 1 2016 2016
CUI: C0001624
Disease: Adrenal Gland Neoplasms
Adrenal Gland Neoplasms
group Neoplasms; Endocrine System Diseases Neoplastic Process 94 0.010 None 1.000 1 2006 2006
MYELOPROLIFERATIVE SYNDROME, TRANSIENT
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 105 9 0.010 None 1.000 1 2011 2011
Leukocyte adhesion deficiency type 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 114 26 0.020 None 1.000 2 2013 2014
CUI: C1136033
Disease: Cutaneous Mastocytosis
Cutaneous Mastocytosis
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 127 18 0.010 None 1.000 1 2009 2009
CUI: C0008495
Disease: Chorioamnionitis
Chorioamnionitis
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 132 2 0.010 None 1.000 1 2011 2011
CUI: C1862382
Disease: SVEINSSON CHORIORETINAL ATROPHY
SVEINSSON CHORIORETINAL ATROPHY
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 139 30 0.010 None 1.000 1 2017 2017
CUI: C0152459
Disease: Linear atrophy
Linear atrophy
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 149 6 0.010 None 1.000 1 2018 2018
Respiratory Distress Syndrome, Newborn
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases Disease or Syndrome 177 37 0.010 None 1.000 1 2018 2018
CUI: C0243038
Disease: Carcinoma, Lewis Lung
Carcinoma, Lewis Lung
disease Neoplasms Neoplastic Process; Experimental Model of Disease 188 0.010 None 1.000 1 2011 2011
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss
phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases Sign or Symptom 235 11 0.010 None 1.000 1 2018 2018
Leukoencephalopathy, Progressive Multifocal
disease Infections; Nervous System Diseases Disease or Syndrome 240 4 0.010 None 1.000 1 2014 2014