TP53, tumor protein p53, 7157

N. diseases: 84; N. variants: 390
Source: CLINVAR ×
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: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 26 35 0.100 None 0 1
CUI: C1328587
Disease: Panhypogammaglobulinemia
Panhypogammaglobulinemia
phenotype Finding 1 2 0.100 None 0 2
CUI: C1266184
Disease: Atypical Teratoid Rhabdoid Tumor
Atypical Teratoid Rhabdoid Tumor
disease Neoplasms Neoplastic Process 1 1 0.100 None 0 1
CUI: C0878638
Disease: Abnormality of the tongue
Abnormality of the tongue
phenotype Finding 2 2 0.100 None 0 1
CUI: C1857641
Disease: Severe postnatal growth retardation
Severe postnatal growth retardation
phenotype Finding 2 5 0.100 None 0 2
CUI: C0349588
Disease: Short stature
Short stature
phenotype Finding 190 292 0.100 None 0 1
CUI: C4748488
Disease: BONE MARROW FAILURE SYNDROME 5
BONE MARROW FAILURE SYNDROME 5
disease Disease or Syndrome 1 2 0.400 limited 0 2
Malignant neoplasm of large intestine
disease Digestive System Diseases; Neoplasms Neoplastic Process 3 7 0.100 None 0 2
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
disease Mental Disorders Mental or Behavioral Dysfunction 26 25 0.100 None 0 1
CUI: C2750850
Disease: GLIOMA SUSCEPTIBILITY 1
GLIOMA SUSCEPTIBILITY 1
phenotype Finding 2 7 0.400 None 0 6
CUI: C0221217
Disease: Neck webbing
Neck webbing
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 11 19 0.100 None 0 1
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
phenotype Finding 160 246 0.100 None 0 2
Vulvar Adenocarcinoma of Mammary Gland Type
disease Neoplastic Process 2 2 0.100 None 0 1
Small cell carcinoma of the ovary, hypercalcemic type
phenotype Neoplasms Finding 1 1 0.100 None 0 1
CUI: C1334655
Disease: Mediastinal Germ Cell Tumor
Mediastinal Germ Cell Tumor
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 2 2 0.100 None 0 1
BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 7
disease Finding 1 7 0.400 None 0 7
ADRENOCORTICAL CARCINOMA, HEREDITARY
disease Neoplasms; Endocrine System Diseases Neoplastic Process 1 6 0.620 None 1.000 0 6 1994 2001
CUI: C0023462
Disease: Acute Megakaryocytic Leukemias
Acute Megakaryocytic Leukemias
disease Neoplasms Neoplastic Process 4 7 0.120 None 1.000 0 1 2000 2012
CUI: C0018671
Disease: Head and Neck Neoplasms
Head and Neck Neoplasms
group Neoplasms Neoplastic Process 4 6 0.500 None 1.000 1 1 2001 2014
CUI: C1859973
Disease: Adrenocortical Carcinoma, Pediatric
Adrenocortical Carcinoma, Pediatric
disease Neoplasms; Endocrine System Diseases Neoplastic Process 1 2 0.110 None 1.000 0 2 2015 2015
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 26 152 0.100 None 1.000 1 43 2016 2016
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
Serous cystadenocarcinoma ovary
disease Neoplasms Neoplastic Process 9 99 0.110 None 1.000 1 77 1999 2016
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
Nasopharyngeal Neoplasms
group Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases Neoplastic Process 6 17 0.410 None 1.000 1 5 2005 2016
Papillary renal cell carcinoma, sporadic
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 11 30 0.100 None 1.000 1 6 2016 2016
CUI: C2749484
Disease: NEUROBLASTOMA, SUSCEPTIBILITY TO
NEUROBLASTOMA, SUSCEPTIBILITY TO
phenotype Finding 11 34 0.100 None 1.000 1 2 2016 2016