PDLIM3, PDZ and LIM domain 3, 27295

N. diseases: 116; N. variants: 4
Source: BEFREE ×
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: C0041948
Disease: Uremia
Uremia
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 89 2 0.010 None 1.000 1 2015 2015
CUI: C0268413
Disease: Adult hypophosphatasia (disorder)
Adult hypophosphatasia (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 9 4 0.010 None 1.000 1 2005 2005
CUI: C0276623
Disease: Chronic viral hepatitis
Chronic viral hepatitis
disease Digestive System Diseases Disease or Syndrome 59 8 0.010 None 1.000 1 2017 2017
Liver and Intrahepatic Biliary Tract Carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 1394 73 0.010 None 1.000 1 2019 2019
CUI: C0282193
Disease: Iron Overload
Iron Overload
disease Nutritional and Metabolic Diseases Disease or Syndrome 235 53 0.010 None 1.000 1 2009 2009
CUI: C0302142
Disease: Deformity
Deformity
group Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Anatomical Abnormality 350 26 0.010 None 1.000 1 2019 2019
CUI: C0339510
Disease: Vitelliform Macular Dystrophy
Vitelliform Macular Dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 73 40 0.010 None 1.000 1 2019 2019
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver
disease Digestive System Diseases; Neoplasms Neoplastic Process 1510 88 0.010 None 1.000 1 2019 2019
CUI: C0410158
Disease: Muscle damage
Muscle damage
phenotype Acquired Abnormality 163 4 0.010 None 1.000 1 2019 2019
CUI: C0432123
Disease: Sagittal craniosynostosis
Sagittal craniosynostosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 19 4 0.010 None 1.000 1 2015 2015
CUI: C0265534
Disease: Scaphycephaly
Scaphycephaly
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 14 4 0.010 None 1.000 1 2015 2015
Systemic Inflammatory Response Syndrome
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 179 9 0.010 None 1.000 1 2018 2018
CUI: C0234119
Disease: Neuromuscular inhibition
Neuromuscular inhibition
disease Disease or Syndrome 72 2 0.010 None 1.000 1 2019 2019
CUI: C0080032
Disease: Pleural Effusion, Malignant
Pleural Effusion, Malignant
disease Neoplasms; Respiratory Tract Diseases Disease or Syndrome 115 6 0.010 None 1.000 1 2020 2020
CUI: C0151825
Disease: Bone pain
Bone pain
phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Sign or Symptom 75 0.010 None 1.000 1 2018 2018
CUI: C0151846
Disease: Periosteal Disorder
Periosteal Disorder
disease Musculoskeletal Diseases Disease or Syndrome 80 0.010 None 1.000 1 2020 2020
CUI: C0162557
Disease: Liver Failure, Acute
Liver Failure, Acute
disease Digestive System Diseases Disease or Syndrome 236 14 0.010 None 1.000 1 2020 2020
CUI: C0205823
Disease: Pleomorphic Lipoma
Pleomorphic Lipoma
disease Neoplasms Neoplastic Process 11 0.010 None 1.000 1 2000 2000
CUI: C0205851
Disease: Germ cell tumor
Germ cell tumor
disease Neoplasms Neoplastic Process 269 5 0.010 None 1.000 1 1989 1989
CUI: C0220620
Disease: Gastrointestinal Carcinoid Tumor
Gastrointestinal Carcinoid Tumor
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 323 13 0.010 None 1.000 1 2017 2017
Metastatic castration-resistant prostate cancer
disease Neoplastic Process 140 2 0.010 None 1.000 1 2018 2018
Congenital contractural arachnodactyly
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 557 20 0.010 None 1.000 1 2017 2017
CUI: C0451641
Disease: Urolithiasis
Urolithiasis
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 59 16 0.010 None 1.000 1 2017 2017
CUI: C0476273
Disease: Respiratory distress
Respiratory distress
phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Sign or Symptom 84 6 0.010 None 1.000 1 2018 2018
CUI: C0497156
Disease: Lymphadenopathy
Lymphadenopathy
phenotype Hemic and Lymphatic Diseases Disease or Syndrome 148 1 0.010 None 1.000 1 2018 2018