ZFP36, ZFP36 ring finger protein, 7538

N. diseases: 99; 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: C0026996
Disease: Myeloid hyperplasia
Myeloid hyperplasia 		disease Disease or Syndrome 6 0.010 1.000 1 2005 2005
CUI: C0205788
Disease: Histiocytoid hemangioma
Histiocytoid hemangioma 		disease Neoplasms Neoplastic Process 9 0.020 0.500 2 2015 2015
CUI: C1848533
Disease: Ataxia with vitamin E deficiency
Ataxia with vitamin E deficiency 		disease Nervous System Diseases; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms Disease or Syndrome 12 23 0.020 1.000 2 2006 2013
CUI: C0263477
Disease: Female pattern alopecia (disorder)
Female pattern alopecia (disorder) 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 13 0.300 1 2005 2005
CUI: C1268935
Disease: Congenital Thrombotic Thrombocytopenic Purpura
Congenital Thrombotic Thrombocytopenic Purpura 		disease Hemic and Lymphatic Diseases; Pathological Conditions, Signs and Symptoms Disease or Syndrome 14 54 0.010 1.000 1 2011 2011
CUI: C0086873
Disease: Pseudopelade
Pseudopelade 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 16 0.300 1 2005 2005
CUI: C0029227
Disease: Delirium, Dementia, Amnestic, Cognitive Disorders
Delirium, Dementia, Amnestic, Cognitive Disorders 		group Mental Disorders Mental or Behavioral Dysfunction 29 0.010 1.000 1 2014 2014
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 30 2 0.300 1 2005 2005
CUI: C0034155
Disease: Purpura, Thrombotic Thrombocytopenic
Purpura, Thrombotic Thrombocytopenic 		disease Hemic and Lymphatic Diseases; Pathological Conditions, Signs and Symptoms Disease or Syndrome 39 10 0.010 1.000 1 1988 1988
CUI: C0392164
Disease: Pulmonary Cystic Fibrosis
Pulmonary Cystic Fibrosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases Disease or Syndrome 42 0.010 1.000 1 2009 2009
CUI: C4041080
Disease: Neurocognitive Disorders
Neurocognitive Disorders 		group Mental Disorders Mental or Behavioral Dysfunction 43 0.010 1.000 1 2014 2014
CUI: C0012739
Disease: Disseminated Intravascular Coagulation
Disseminated Intravascular Coagulation 		disease Hemic and Lymphatic Diseases Disease or Syndrome 45 0.010 1.000 1 1999 1999
CUI: C0162323
Disease: Polyarthritis
Polyarthritis 		disease Musculoskeletal Diseases Disease or Syndrome 48 1 0.310 1.000 2 2005 2005
CUI: C0242510
Disease: Drug usage
Drug usage 		phenotype Mental or Behavioral Dysfunction 51 10 0.010 1.000 1 2004 2004
CUI: C0162311
Disease: Androgenetic Alopecia
Androgenetic Alopecia 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 59 745 0.300 1 2005 2005
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		disease Disease or Syndrome 59 17 0.010 1.000 1 2009 2009
CUI: C0019061
Disease: Hemolytic-Uremic Syndrome
Hemolytic-Uremic Syndrome 		disease Female Urogenital Diseases and Pregnancy Complications; Hemic and Lymphatic Diseases; Male Urogenital Diseases Disease or Syndrome 61 3 0.010 1.000 1 1988 1988
CUI: C1510885
Disease: Angiogenic Switch
Angiogenic Switch 		disease Neoplastic Process 74 0.010 1.000 1 2008 2008
CUI: C0037221
Disease: Situs Inversus
Situs Inversus 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 83 5 0.010 1.000 1 2014 2014
CUI: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies 		disease Endocrine System Diseases; Eye Diseases; Immune System Diseases Disease or Syndrome 91 28 0.010 1.000 1 2015 2015
CUI: C1519689
Disease: Tumor Promotion
Tumor Promotion 		phenotype Neoplastic Process 107 2 0.010 1.000 1 2014 2014
CUI: C0020507
Disease: Hyperplasia
Hyperplasia 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 122 0.300 1 2005 2005
CUI: C0007682
Disease: CNS disorder
CNS disorder 		group Nervous System Diseases Disease or Syndrome 123 2 0.010 1.000 1 2014 2014
CUI: C0947751
Disease: Vascular inflammations
Vascular inflammations 		phenotype Disease or Syndrome 141 1 0.010 1.000 1 2013 2013
CUI: C0027121
Disease: Myositis
Myositis 		disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 142 11 0.010 1.000 1 2012 2012