TP53, tumor protein p53, 7157

N. diseases: 2494; N. variants: 527
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: C0028259
Disease: Nodule
Nodule
phenotype Acquired Abnormality 278 19 0.100 None 1.000 13 1992 2018
CUI: C0242621
Disease: Isochromosomes
Isochromosomes
phenotype Pathological Conditions, Signs and Symptoms Acquired Abnormality 75 2 0.100 None 0.909 11 1992 2018
CUI: C0022548
Disease: Keloid
Keloid
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Acquired Abnormality 165 15 0.040 None 1.000 4 3 1998 2017
CUI: C0333307
Disease: Superficial ulcer
Superficial ulcer
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 242 10 0.040 None 1.000 4 2004 2013
CUI: C0004277
Disease: Tooth Attrition
Tooth Attrition
disease Stomatognathic Diseases Acquired Abnormality 66 5 0.030 None 1.000 3 2000 2018
CUI: C0086543
Disease: Cataract
Cataract
disease Eye Diseases Acquired Abnormality 878 124 0.030 None 1.000 3 1 2016 2019
CUI: C0162810
Disease: Cicatrix, Hypertrophic
Cicatrix, Hypertrophic
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 185 3 0.030 None 1.000 3 2004 2009
CUI: C0740391
Disease: Middle Cerebral Artery Occlusion
Middle Cerebral Artery Occlusion
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 626 0.030 None 1.000 3 2015 2019
CUI: C0036280
Disease: Burn scar
Burn scar
disease Pathological Conditions, Signs and Symptoms; Wounds and Injuries Acquired Abnormality 11 0.020 None 1.000 2 1997 1999
CUI: C0086501
Disease: Keratoma
Keratoma
disease Skin and Connective Tissue Diseases Acquired Abnormality 5 0.300 None 1.000 2 2006 2017
CUI: C0276262
Disease: Verruca plana
Verruca plana
disease Infections; Skin and Connective Tissue Diseases Acquired Abnormality 4 0.020 None 1.000 2 1995 2012
CUI: C0332853
Disease: Anastomosis
Anastomosis
disease Acquired Abnormality 155 2 0.020 None 1.000 2 2000 2007
CUI: C0033844
Disease: Pseudotumor
Pseudotumor
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 11 0.010 None 1.000 1 2006 2006
CUI: C0036646
Disease: Age-related cataract
Age-related cataract
disease Eye Diseases Acquired Abnormality 92 15 0.010 None < 0.001 1 2016 2016
CUI: C0545034
Disease: pituitary giant
pituitary giant
disease Acquired Abnormality 1 0.010 None < 0.001 1 2011 2011
CUI: C0152459
Disease: Linear atrophy
Linear atrophy
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 149 6 0.100 None 0
CUI: C0032584
Disease: polyps
polyps
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 390 18 0.100 None 0.933 15 1993 2006
CUI: C0009376
Disease: Colonic Polyps
Colonic Polyps
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 69 8 0.030 None 1.000 3 2001 2018
CUI: C4531138
Disease: Short telomere length
Short telomere length
phenotype Anatomical Abnormality 12 1 0.030 None 1.000 3 2013 2019
CUI: C0014511
Disease: Epithelial cyst
Epithelial cyst
phenotype Neoplasms Anatomical Abnormality 38 0.020 None 1.000 2 1999 2003
CUI: C2919945
Disease: Cavernous Hemangioma of Brain
Cavernous Hemangioma of Brain
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Anatomical Abnormality 127 43 0.020 None 0.500 2 2004 2019
CUI: C0003855
Disease: Arteriovenous fistula
Arteriovenous fistula
phenotype Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Anatomical Abnormality 93 8 0.010 None 1.000 1 2018 2018
CUI: C0037157
Disease: Simple cyst
Simple cyst
disease Pathological Conditions, Signs and Symptoms; Neoplasms Anatomical Abnormality 3 0.010 None 1.000 1 2010 2010
CUI: C0206740
Disease: Calcifying Odontogenic Cyst
Calcifying Odontogenic Cyst
disease Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases Anatomical Abnormality 15 1 0.010 None 1.000 1 2010 2010
CUI: C0269155
Disease: Germinal inclusion cyst of ovary
Germinal inclusion cyst of ovary
disease Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Anatomical Abnormality 3 0.010 None 1.000 1 2003 2003