PLB1, phospholipase B1, 151056

N. diseases: 219; N. variants: 10
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: C4302857
Disease: Malignancy-associated membranous nephropathy
Malignancy-associated membranous nephropathy 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C0391820
Disease: Gouty nephropathy
Gouty nephropathy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 5 0.010 None 1.000 1 2019 2019
CUI: C3496228
Disease: Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia
Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 5 12 0.010 None 1.000 1 2016 2016
CUI: C4517377
Disease: Coenzyme A synthase protein associated neurodegeneration
Coenzyme A synthase protein associated neurodegeneration 		disease Nutritional and Metabolic Diseases Disease or Syndrome 5 0.010 None 1.000 1 2016 2016
CUI: C4054543
Disease: Membranous Lupus Nephritis
Membranous Lupus Nephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 6 0.010 None 1.000 1 2019 2019
CUI: C1260881
Disease: Allergic bronchitis
Allergic bronchitis 		disease Infections; Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 8 2 0.010 None 1.000 1 2013 2013
CUI: C3711384
Disease: Distal Hereditary Motor Neuropathy, Type II
Distal Hereditary Motor Neuropathy, Type II 		disease Nervous System Diseases Disease or Syndrome 8 2 0.010 None 1.000 1 1997 1997
CUI: C0342286
Disease: Woodhouse Sakati syndrome
Woodhouse Sakati syndrome 		disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases; Endocrine System Diseases; Mental Disorders; Behavior and Behavior Mechanisms; Cardiovascular Diseases Disease or Syndrome 9 11 0.010 None 1.000 1 2016 2016
CUI: C2674616
Disease: FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder)
FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms Disease or Syndrome 10 7 0.010 None 1.000 1 1996 1996
CUI: C1847640
Disease: KUFOR-RAKEB SYNDROME
KUFOR-RAKEB SYNDROME 		disease Nervous System Diseases Disease or Syndrome 11 16 0.010 None 1.000 1 2016 2016
CUI: C0281902
Disease: maladjustment
maladjustment 		phenotype Mental or Behavioral Dysfunction 13 0.010 None 1.000 1 2005 2005
CUI: C1328577
Disease: Empty follicle syndrome
Empty follicle syndrome 		disease Disease or Syndrome 14 1 0.010 None 1.000 1 2006 2006
CUI: C0009021
Disease: Clonorchiasis
Clonorchiasis 		disease Infections Disease or Syndrome 15 0.010 None 1.000 1 2007 2007
CUI: C0270724
Disease: Infantile Neuroaxonal Dystrophy
Infantile Neuroaxonal Dystrophy 		disease Nervous System Diseases Disease or Syndrome 17 25 0.070 None 1.000 7 2010 2016
CUI: C1853578
Disease: Neuroferritinopathy
Neuroferritinopathy 		disease Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 17 5 0.010 None 1.000 1 2016 2016
CUI: C0404521
Disease: Infective vaginitis
Infective vaginitis 		disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Infections Disease or Syndrome 18 0.010 None 1.000 1 2003 2003
CUI: C3550973
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 19 28 0.010 None 1.000 1 2016 2016
CUI: C0018523
Disease: Hallervorden-Spatz Syndrome
Hallervorden-Spatz Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 22 42 0.020 None 1.000 2 2011 2011
CUI: C0268575
Disease: Isovaleryl-CoA dehydrogenase deficiency
Isovaleryl-CoA dehydrogenase deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 22 55 0.010 None 1.000 1 2018 2018
CUI: C2350019
Disease: Solitary Pulmonary Nodule
Solitary Pulmonary Nodule 		disease Respiratory Tract Diseases Neoplastic Process 25 0.010 None 1.000 1 2018 2018
CUI: C0018915
Disease: Hemangioendothelioma
Hemangioendothelioma 		disease Neoplasms Neoplastic Process 26 0.010 None 1.000 1 1996 1996
CUI: C0015371
Disease: Extrapyramidal Disorders
Extrapyramidal Disorders 		group Nervous System Diseases Disease or Syndrome 27 1 0.010 None 1.000 1 2011 2011
CUI: C3203653
Disease: IgG4-Related Sclerosing Disease
IgG4-Related Sclerosing Disease 		disease Immune System Diseases Disease or Syndrome 30 0.010 None 1.000 1 2019 2019
CUI: C0023521
Disease: Globoid cell leukodystrophy
Globoid cell leukodystrophy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 35 111 0.010 None 1.000 1 2006 2006
CUI: C0178264
Disease: Inflammatory disease of the central nervous system
Inflammatory disease of the central nervous system 		group Nervous System Diseases Disease or Syndrome 36 0.010 None 1.000 1 2018 2018