PARP1, poly(ADP-ribose) polymerase 1, 142

N. diseases: 565; N. variants: 23
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: C1707400
Disease: Classic medulloblastoma
Classic medulloblastoma 		disease Neoplasms Neoplastic Process 3 0.010 None 1.000 1 2009 2009
CUI: C1266180
Disease: Large cell medulloblastoma
Large cell medulloblastoma 		disease Neoplasms Neoplastic Process 4 0.010 None 1.000 1 2009 2009
CUI: C1562312
Disease: Estrogen receptor positive tumor
Estrogen receptor positive tumor 		disease Neoplastic Process 4 0.010 None 1.000 1 2019 2019
CUI: C3150658
Disease: WARSAW BREAKAGE SYNDROME
WARSAW BREAKAGE SYNDROME 		disease Disease or Syndrome 4 5 0.010 None 1.000 1 2015 2015
CUI: C0015697
Disease: Arterial Fatty Streak
Arterial Fatty Streak 		phenotype Pathological Conditions, Signs and Symptoms Acquired Abnormality 5 0.300 None 1.000 1 2009 2009
CUI: C0264956
Disease: Atheroma
Atheroma 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 5 0.300 None 1.000 1 2009 2009
CUI: C1850554
Disease: Atelosteogenesis type 2
Atelosteogenesis type 2 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 5 34 0.010 None 1.000 1 2018 2018
CUI: C2936350
Disease: Plaque, Atherosclerotic
Plaque, Atherosclerotic 		phenotype Pathological Conditions, Signs and Symptoms Body Substance 5 0.300 None 1.000 1 2009 2009
CUI: C4525546
Disease: Chicken Lymphoma
Chicken Lymphoma 		disease Neoplastic Process 5 0.010 None 1.000 1 2020 2020
CUI: C1862112
Disease: BRACHYDACTYLY, TYPE B1
BRACHYDACTYLY, TYPE B1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 6 8 0.010 None 1.000 1 2019 2019
CUI: C0919645
Disease: Tumour ulceration
Tumour ulceration 		disease Neoplastic Process 7 2 0.010 None 1.000 1 2014 2014
CUI: C1112338
Disease: Apoptotic DNA damage
Apoptotic DNA damage 		disease Disease or Syndrome 7 0.010 None 1.000 1 2010 2010
CUI: C0238097
Disease: Cytomegalovirus encephalitis
Cytomegalovirus encephalitis 		disease Infections; Nervous System Diseases Disease or Syndrome 8 0.010 None 1.000 1 2017 2017
CUI: C0347390
Disease: Skin Papilloma
Skin Papilloma 		disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 8 0.010 None 1.000 1 2005 2005
CUI: C1112474
Disease: Small cell carcinoma of esophagus
Small cell carcinoma of esophagus 		disease Neoplastic Process 8 5 0.010 None 1.000 1 1 2015 2015
CUI: C2936351
Disease: Fibroatheroma
Fibroatheroma 		disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 8 0.300 None 1.000 1 2009 2009
CUI: C1862322
Disease: Ovalocytosis, Malaysian-Melanesian-Filipino Type
Ovalocytosis, Malaysian-Melanesian-Filipino Type 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 9 5 0.010 None 1.000 1 2001 2001
CUI: C4054891
Disease: Grade III Chondrosarcoma
Grade III Chondrosarcoma 		disease Neoplasms Neoplastic Process 9 0.010 None 1.000 1 2019 2019
CUI: C0278725
Disease: Small cell lung cancer limited stage
Small cell lung cancer limited stage 		disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 14 2 0.010 None 1.000 1 2014 2014
CUI: C1333992
Disease: Hereditary Ovarian Carcinoma
Hereditary Ovarian Carcinoma 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Neoplastic Process 14 0.010 None 1.000 1 2018 2018
CUI: C2931673
Disease: Ceroid lipofuscinosis, neuronal 1, infantile
Ceroid lipofuscinosis, neuronal 1, infantile 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 14 1 0.300 None 1.000 1 2011 2011
CUI: C0263477
Disease: Female pattern alopecia (disorder)
Female pattern alopecia (disorder) 		phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 15 0.300 None 1.000 1 2010 2010
CUI: C4324396
Disease: Immune-mediated hepatitis
Immune-mediated hepatitis 		disease Disease or Syndrome 15 0.010 None 1.000 1 2012 2012
CUI: C0268095
Disease: Keshan disease
Keshan disease 		disease Infections; Cardiovascular Diseases Disease or Syndrome 17 1 0.010 None 1.000 1 2018 2018
CUI: C1840333
Disease: Barakat syndrome
Barakat syndrome 		disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases; Endocrine System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 17 9 0.010 None 1.000 1 2017 2017