Proteus-Like Syndrome (disorder)
|
0.740 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Proteus-Like Syndrome (disorder)
|
0.740 |
CausalMutation
|
disease |
CLINVAR |
Appendectomy, tonsillectomy, and neoplasia.
|
1097835 |
1975 |
Proteus-Like Syndrome (disorder)
|
0.740 |
CausalMutation
|
disease |
CLINVAR |
Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease.
|
9259288 |
1997 |
Proteus-Like Syndrome (disorder)
|
0.740 |
CausalMutation
|
disease |
CLINVAR |
Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis.
|
9399897 |
1997 |
Proteus-Like Syndrome (disorder)
|
0.740 |
CausalMutation
|
disease |
CLINVAR |
Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTEN.
|
10353779 |
1999 |
Proteus-Like Syndrome (disorder)
|
0.740 |
GeneticVariation
|
disease |
CLINVAR |
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.
|
10400993 |
1999 |
Proteus-Like Syndrome (disorder)
|
0.740 |
CausalMutation
|
disease |
CLINVAR |
The tumor-suppressor activity of PTEN is regulated by its carboxyl-terminal region.
|
10468583 |
1999 |
Proteus-Like Syndrome (disorder)
|
0.740 |
GermlineCausalMutation
|
disease |
ORPHANET |
Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis.
|
10749983 |
2000 |
Proteus-Like Syndrome (disorder)
|
0.740 |
CausalMutation
|
disease |
CLINVAR |
Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis.
|
10749983 |
2000 |
Proteus-Like Syndrome (disorder)
|
0.740 |
CausalMutation
|
disease |
CLINVAR |
Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromes.
|
11476841 |
2001 |
Proteus-Like Syndrome (disorder)
|
0.740 |
Biomarker
|
disease |
CTD_human |
A novel germline mutation of the PTEN gene in a patient with macrocephaly, ventricular dilatation, and features of VATER association.
|
11748304 |
2001 |
Proteus-Like Syndrome (disorder)
|
0.740 |
Biomarker
|
disease |
CTD_human |
Germline mutation of the tumour suppressor PTEN in Proteus syndrome.
|
12471211 |
2002 |
Proteus-Like Syndrome (disorder)
|
0.740 |
GeneticVariation
|
disease |
BEFREE |
Germline PTEN mutations have been found to occur in 80% of classic Cowden syndrome (CS), 60% of Bannayan-Riley-Ruvalcaba syndrome (BRRS), up to 20% of Proteus syndrome (PS), and approximately 50% of a Proteus-like syndrome (PSL).
|
12938083 |
2003 |
Proteus-Like Syndrome (disorder)
|
0.740 |
GeneticVariation
|
disease |
CLINVAR |
Germline inactivation of PTEN and dysregulation of the phosphoinositol-3-kinase/Akt pathway cause human Lhermitte-Duclos disease in adults.
|
14566704 |
2003 |
Proteus-Like Syndrome (disorder)
|
0.740 |
CausalMutation
|
disease |
CLINVAR |
Analysis of PTEN gene mutations in Korean patients with Cowden syndrome and polyposis syndrome.
|
16007494 |
2005 |
Proteus-Like Syndrome (disorder)
|
0.740 |
Biomarker
|
disease |
CTD_human |
Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly.
|
17427195 |
2007 |
Proteus-Like Syndrome (disorder)
|
0.740 |
CausalMutation
|
disease |
CLINVAR |
Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriers.
|
17526800 |
2007 |
Proteus-Like Syndrome (disorder)
|
0.740 |
GeneticVariation
|
disease |
CLINVAR |
In vivo functional analysis of the counterbalance of hyperactive phosphatidylinositol 3-kinase p110 catalytic oncoproteins by the tumor suppressor PTEN.
|
17942903 |
2007 |
Proteus-Like Syndrome (disorder)
|
0.740 |
CausalMutation
|
disease |
CLINVAR |
Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome clinical features.
|
21659347 |
2011 |
Proteus-Like Syndrome (disorder)
|
0.740 |
GeneticVariation
|
disease |
CLINVAR |
A comprehensive functional analysis of PTEN mutations: implications in tumor- and autism-related syndromes.
|
21828076 |
2011 |
Proteus-Like Syndrome (disorder)
|
0.740 |
CausalMutation
|
disease |
CLINVAR |
Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterations.
|
21956414 |
2011 |
Proteus-Like Syndrome (disorder)
|
0.740 |
GeneticVariation
|
disease |
CLINVAR |
Lifetime cancer risks in individuals with germline PTEN mutations.
|
22252256 |
2012 |
Proteus-Like Syndrome (disorder)
|
0.740 |
GeneticVariation
|
disease |
CLINVAR |
Elevated plasma succinate in PTEN, SDHB, and SDHD mutation-positive individuals.
|
22261759 |
2012 |
Proteus-Like Syndrome (disorder)
|
0.740 |
CausalMutation
|
disease |
CLINVAR |
Autoimmunity, intestinal lymphoid hyperplasia, and defects in mucosal B-cell homeostasis in patients with PTEN hamartoma tumor syndrome.
|
22266152 |
2012 |
Proteus-Like Syndrome (disorder)
|
0.740 |
GeneticVariation
|
disease |
CLINVAR |
Estimate of de novo mutation frequency in probands with PTEN hamartoma tumor syndrome.
|
22595938 |
2012 |