LMLN, leishmanolysin like peptidase, 89782

N. diseases: 138; N. variants: 2
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: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.090 None 1.000 9 1993 2019
CUI: C0278488
Disease: Carcinoma breast stage IV
Carcinoma breast stage IV
disease Neoplastic Process 573 14 0.010 None 1.000 1 2012 2012
Total iron binding capacity function
phenotype Clinical Attribute 20 35 0.100 None 1.000 1 1 2017 2017
CUI: C0702266
Disease: Basophilia
Basophilia
disease Disease or Syndrome 12 0.010 None 1.000 1 1991 1991
Iron binding capacity total measurement
phenotype Laboratory Procedure 20 35 0.100 None 1.000 1 1 2017 2017
CUI: C1378050
Disease: Oncocytic Neoplasm
Oncocytic Neoplasm
disease Neoplastic Process 105 2 0.010 None 1.000 1 2003 2003
CUI: C3826128
Disease: Infection in children
Infection in children
disease Disease or Syndrome 29 5 0.010 None 1.000 1 2012 2012
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.010 None 1.000 1 2010 2010
CUI: C4732730
Disease: Blood spots
Blood spots
disease Disease or Syndrome 117 0.010 None 1.000 1 2011 2011
CUI: C0003467
Disease: Anxiety
Anxiety
disease Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1048 287 0.010 None 1.000 1 2019 2019
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
disease Cardiovascular Diseases Disease or Syndrome 773 243 0.010 None 1.000 1 2013 2013
CUI: C0005411
Disease: Biliary Atresia
Biliary Atresia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 184 32 0.010 None 1.000 1 2002 2002
Congenital atresia of extrahepatic bile duct
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 172 19 0.010 None 1.000 1 2002 2002
CUI: C1562061
Disease: Microspherophakia
Microspherophakia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 9 0.010 None 1.000 1 2009 2009
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 86 37 0.010 None < 0.001 1 2009 2009
CUI: C0472762
Disease: Alpha trait thalassemia
Alpha trait thalassemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 10 3 0.010 None 1.000 1 2015 2015
CUI: C1456873
Disease: alpha^+^ Thalassemia
alpha^+^ Thalassemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 92 16 0.010 None < 0.001 1 2009 2009
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms Neoplastic Process 270 139 0.010 None 1.000 1 2014 2014
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 94 135 0.010 None 1.000 1 2012 2012
Deficiency of glucose-6-phosphate dehydrogenase
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 75 20 0.010 None < 0.001 1 2009 2009
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 185 8 0.010 None 1.000 1 2012 2012
CUI: C0085695
Disease: Chronic gastritis
Chronic gastritis
disease Digestive System Diseases Disease or Syndrome 114 11 0.010 None 1.000 1 2013 2013
CUI: C0162557
Disease: Liver Failure, Acute
Liver Failure, Acute
disease Digestive System Diseases Disease or Syndrome 282 21 0.010 None 1.000 1 1994 1994
CUI: C0266239
Disease: Congenital anomaly of bile ducts
Congenital anomaly of bile ducts
group Digestive System Diseases Congenital Abnormality 4 0.010 None < 0.001 1 2002 2002
CUI: C0021832
Disease: Intestinal Diseases, Parasitic
Intestinal Diseases, Parasitic
group Digestive System Diseases; Infections Disease or Syndrome 19 0.010 None 1.000 1 2015 2015