Disease #00001

Official abbreviation Lynch Syndrome
Name cancer, colorectal, nonpolyposis, hereditary, type 1 (Lynch syndrome, HNPCC-1)
OMIM ID 120435
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 1367
Phenotype entries for this disease 429
Associated with 6 genes MLH1, MLH3, MSH2, MSH3, MSH6, PMS2
Associated tissues -
Disease features -
Remarks -


Individuals

1367 entries on 14 pages. Showing entries 1 - 100.
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Pedigree information available     

Family History     

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Disease     

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00001847 - M - - - - 2 gen & 3 cases CRC 54,66,47; 4 Cases of Breast Ca ( Amsterdam II) CRC Lynch Syndrome Adenocarcinoma MLH1 MLH1 1 1 Ruth Armstrong
00001848 - F - - - - 2 gen & 3 cases CRC 54,66,47; 4 Cases of Breast Ca ( Amsterdam II) Breast+CRC Lynch Syndrome Bowel Cancer; Breast-63y; Colon 66y MLH1, MSH2, MSH6 MLH1 1 1 Ruth Armstrong
00001849 - F - - - - 2 gen; 1xEndometrial 61;1 case CRC@64 Endometrial Lynch Syndrome Endometrial Cancer, Follicular Lymphoma,Melanoma,Squamous cell carcinoma MLH1, MSH2, MSH6 MSH6 1 1 Ruth Armstrong
00001850 - F - - - - No FH of CRC Endometrial tumour Lynch Syndrome Endometrioid adenocarinoma, MSH6 protein expression: Negative/Abnormal MSH6 MSH6 1 1 Ruth Armstrong
00001851 - M - - - - 3 gen & 6 cases of CRC( Amsterdam II) CRC Lynch Syndrome Adenocarcinoma MSH6 MSH6 2 1 Ruth Armstrong
00001852 - M - - - - 2 Gen(not sucessive); 1x CRC@51;1xStomach Ca@53 CRC Lynch Syndrome Sigmoid mucinous adenocarcinoma, 3xTVA, MSH2 protein expression: weak MSH2, MSH6 MSH2, MSH6 2 1 Ruth Armstrong
00001853 - F - - - - 2 Gen;2 cases CRC 58,42;2xbowel polyps. CRC Lynch Syndrome Transverse Colon adenocarcinoma, >=35 pol MLH1, MSH2, MSH6 MSH6 1 1 Ruth Armstrong
00001854 - F - - - - 2 Gen; 2 cases CRC 55,48;1 case endometrial 71 (Amsterdam II) CRC Lynch Syndrome Rectal Adenocarcinoma MLH1, MSH2, MSH6 MSH6 1 1 Ruth Armstrong
00001855 - F - - - - 2 Gen ;2casesCRC 18,66 CRC Lynch Syndrome Ascending colon adenocarcinoma MLH1, MSH2, MSH6 MSH6 1 1 Ruth Armstrong
00001856 - F UK - - - Mother caecal cancer (untested) at 34y CRC Lynch Syndrome Caecal Adenocarcinoma MLH1, MSH2 MLH1 1 1 Ruth Armstrong
00001857 - F - - - - 2 Gen; 3 Cases CRC 47,75,76 (Amsterdam Criteria II) CRC Lynch Syndrome Ascending Colon adenocarcinoma MLH1, MSH2 MLH1 1 1 Ruth Armstrong
00001858 - F - - - - 1 Case , sebaceous adenoma Sebaceous adenoma Lynch Syndrome Sebaceous adenoma, 1 dysplastic polyp MSH2 MSH2 1 1 Ruth Armstrong
00001859 - F - - - - 2 Gen;?2 sides of family?;3 Cases CRC 39,54,89; CRC Lynch Syndrome Sigmoid Adenocarcinoma MLH1, MSH2 MLH1 1 1 Ruth Armstrong
00001860 - M - - - - 4 Gen; 6 cases CRC 39,42,35,58,42,78, 1 case Womb Ca 58, 1 Case Stomach Ca 65 (Amsterdam II) CRC Lynch Syndrome Ascending Colon Adenocarcinoma MLH1, MSH2 MLH1 1 1 Ruth Armstrong
00001862 - M - - - - 2 Gen;3 Cases CRC 40,45,70 (Amsterdam II Criteria) CRC Lynch Syndrome Rectal Adenocarcinoma MLH1, MSH2 MLH1 1 1 Ruth Armstrong
00001863 - F - - - - 3 Gen; 3 Case CRC 54,30,?60's?; 1 Case Endometriod Ca 46; (Amsterdam II) Endometrial Ca Lynch Syndrome Endometriod Carcinoma MLH1, MSH2 MLH1 1 1 Ruth Armstrong
00001864 - F - - - - 3 Gen;4 case CRC 77,75,39,60; 1 case stomach Ca 63 (Amsterdam II) CRC Lynch Syndrome Bowel Cancer MLH1, MSH2 MLH1 1 1 Ruth Armstrong
00001866 - F - - - - 3 gen ; 5 Case CRC 30,30,54,70,70+ (Amsterdam II) CRC + Endometrial Ca Lynch Syndrome Colorectal Carcinoma-30y;Endometrial Ca-51y MLH1, MSH2 MLH1 2 1 Ruth Armstrong
00001867 - F - - - - 3 gen ; 5 Case CRC 30,30,54,70,70+ (Amsterdam II) 2 Mod dys TVAs Lynch Syndrome 2 Adenomas MLH1 - 0 1 Ruth Armstrong
00001868 - F - - - - 2 Gen; 4 Cases CRC 50,62,62,68; 1 Case breast Ca 30 CRC Lynch Syndrome Rectal Carcinoma MLH1, MSH2 MLH1 1 1 Ruth Armstrong
00001869 - M - - Tumour studies done in sister (deceased) - 3 Gen; 3 Cases CRC 31,55,?70's? (Amsterdam II) Family History +TVA Lynch Syndrome Sigmoid mucinous adenocarcinoma MLH1, MSH2 MSH2 1 1 Ruth Armstrong
00001870 - F - - - - 4 Gen;7 cases CRC 27,40,48,52,60,63,68 (Amsterdam II) CRC Lynch Syndrome CRC MLH1, MSH2 MLH1 1 1 Ruth Armstrong
00001871 - F - - - - 4 Gen;7 cases CRC 27,40,48,52,60,63,68 (Amsterdam II) FH + CRC Lynch Syndrome 2 separate CRC-63y,64y MLH1 MLH1 1 1 Ruth Armstrong
00001872 - F - - - - 2 Gen; 4 Cases CRC 40,40,26,50 ( Amsterdam II) CRC Lynch Syndrome Right Colon Adenocarcinoma MLH1 MLH1 1 1 Ruth Armstrong
00001873 - F - - - - 2 Gen; 4 Cases CRC 40,40,26,50 (Amsterdam II) FH Lynch Syndrome No tumour/not symptomatic MLH1 MLH1 1 1 Ruth Armstrong
00001874 - F - - - - 2 Gen; 4 Cases CRC 40,40,26,50 ( Amsterdam II) CRC Lynch Syndrome Colorectal Carcinoma MLH1 MLH1 1 1 Ruth Armstrong
00001875 - F - - - - 2 Gen; 4 Cases CRC 40,40,26,50 (Amsterdam II) FH Lynch Syndrome No tumour/not symptomatic - MLH1 1 1 Ruth Armstrong
00001876 - M - - - - mother with melanoma @63 yr Hepatobillary cancer, leuk and sebaceous tumour Lynch Syndrome Sebaceous tumour MLH1, MSH2, MSH6 MSH6 1 1 Ruth Armstrong
00001877 Liu 2001, Nicolaides 1994, Nicolaides 1994 F - - 4-generation family, 8 affecteds colon cancer, 10 affecteds with other cancers - A+ - Lynch Syndrome HNPCC3, ovarian cancer 43y, colon cancer 51y, endometrial cancer 65y MSH2 MSH2 1 2 John-Paul Plazzer
00001878 Liu 2001 M - - nephew of CW (III4) - - - Lynch Syndrome colorectal cancer 42y MSH2 MSH2 1 1 Johan den Dunnen
00001879 - F - - - - Amsterdam I; pedigree provided. family history CRC, Lynch Syndrome CRC; Unspecified Gynecological Cancer. 21y and 50y; MLH1, MSH2 MLH1 1 1 John Paul Plazzer
00001880 InSiGHT Variant Interpretation Committee April 2016 M - - - - Amsterdam I; pedigree provided family history CRC, Lynch Syndrome crc MLH1, MSH2, MSH6 MLH1 1 1 John Paul Plazzer
00001892 Chika et al, 2015 M Japan - Gan To Kagaku Ryoho. 2015 Nov;42(12):2211-4. [A Family Affected by Lynch Syndrome Caused by MSH6 Germline Mutation]. [Article in Japanese] - From abstract: He had family history of endometrial cancer and gastric cancer(mother), and bladder cancer(father). The Patient met revised Bethesda guidelines. The same MSH6 variant was detected in younger brother. positive fecal occult blood test Lynch Syndrome Sigmoid Cancer MSH6 MSH6 1 1 John Paul Plazzer
00001893 - M Australia - - - He has 3 sisters and a brother; one sister had a choroidal melanoma of the eye at 50. He reports a paternal aunt with breast cancer at an older age. His mother had a melanoma at 80y, he believes her brother may have had a prostate cancer later in life, and a maternal aunt with ovarian serous cystadenocarcinoma in her 70's. - Lynch Syndrome moderately differentiated adenocarcinoma of the rectum at age 50 MLH1, MSH2, MSH6, PMS2 MSH6 1 1 John Paul Plazzer
00002038 - - - - 45 y recurrent 1-2 large tub-vill. Adenomas, no IHC possible. A+ Family: mother 50 y CC, 60 y Rezidiv dedeased, maternal half-uncle 30-40 y CC verstorben, maternal grandmother 60 y CC - A+ - Lynch Syndrome - MLH1 MLH1 1 1 Elke Holinski-Feder
00002039 - - - - no MSA, IHC MLH1 pos., MSH2 pos. MSH6 pos., PMS2 neg. 46 y CC. asc. T3 N1 - father 38 y gastic Ca, 43 y deceased in accident, paternal uncle died at 70 y Pankreatic Ca - Lynch Syndrome - MLH1 MLH1 1 1 Elke Holinski-Feder
00002040 - - - - 76 y Urothelca, MSS, IHC positive in MLH1, MSH2, MLH6, PMS2 n.a. - Amsterdam-old family - Lynch Syndrome - MSH2 MSH2 1 1 Elke Holinski-Feder
00002042 - - - - Suspect of Lynch-Syndrome, Amsterdam positive, index 87297 healthy, mother (MGZ# 3487) CC at 68 y, brother CC 42 y, maternal grandfather gastric cancer, Genes MLH1, MSH2, and PMS2 normal. - Amsterdam positive - Lynch Syndrome - MSH6 MSH6 1 1 Elke Holinski-Feder
00002047 - - - - No tumour testing has been done. - - - Lynch Syndrome - MSH2 MSH2 1 1 Ian Frayling
00002049 InSiGHT Variant Interpretation Committee April 2016 - - - IHC loss of MSH2 and MSH6, MLH1 + PMS2 pos and MSI-H tu index: [C18.6 (51)], [C67 (51)], [C66 (51)], [C65 (51)], [C18.0 (52)] no further variants VUS in MSH2 - Amsterdam 1 positive, 3 additional members with CC at age 46y, 52y and ?y - Lynch Syndrome Malignant neoplasm of bladder (C67), Malignant neoplasm of cecum (C18.0), Malignant neoplasm of descending colon (C18.6), Malignant neoplasm of renal pelvis (C65), Malignant neoplasm of ureter (C66) MSH2 MSH2 1 1 Elke Holinski-Feder
00002050 InSiGHT Variant Interpretation Committee April 2016 - - - MSA not performed, IHC >1-10% for MSH2 + MSH6, >10%/positive for MLH1 + PMS2 - Bethesda 1 positive - Lynch Syndrome Malignant neoplasm of cecum (C18.0) MSH2 MSH2 1 1 Elke Holinski-Feder
00002089 - ? - - InSiGHT LOVDv2 ID:20747; This data has been transferred from InSiGHT LOVDv2 database. - AII-;B?; - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00002131 - F BR - InSiGHT LOVDv2 ID:1010906; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Felipe Silva
00002132 - F BR - InSiGHT LOVDv2 ID:1010908; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Felipe Silva
00002133 silvafelipe - BR - InSiGHT LOVDv2 ID:1010910; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Felipe Silva
00002134 - M BR - InSiGHT LOVDv2 ID:1010911; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Felipe Silva
00002135 - F BR - InSiGHT LOVDv2 ID:1010917; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Felipe Silva
00002144 - F BR - InSiGHT LOVDv2 ID:1010907; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Felipe Silva
00002145 - M BR - InSiGHT LOVDv2 ID:1010909; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Felipe Silva
00002146 - - BR - InSiGHT LOVDv2 ID:1010915; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 3 1 Felipe Silva
00002174 - ? - - InSiGHT LOVDv2 ID:20745; This data has been transferred from InSiGHT LOVDv2 database. - AII-;B?; - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00002250 - ? - - page 1306 for details; missense mutation found in four separate families, each case different MSI or IHC situation; InSiGHT LOVDv2 ID:20775; This data has been transferred from InSiGHT LOVDv2 database. - AII+;B+; - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00002254 - ? - - InSiGHT LOVDv2 ID:20779; This data has been transferred from InSiGHT LOVDv2 database. - AII-;B?; - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00002264 - M BR - InSiGHT LOVDv2 ID:1010913; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Felipe Silva
00002272 Jin et al, 2008 F China - InSiGHT LOVDv2 ID:1013026; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 John Paul Plazzer
00002379 - ? - - InSiGHT LOVDv2 ID:25570; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00002388 - ? DE - InSiGHT LOVDv2 ID:12674; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Beate Dr. Betz
00002389 - ? DE - InSiGHT LOVDv2 ID:12717; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Beate Dr. Betz
00002437 - M IT Caucasian InSiGHT LOVDv2 ID:1013077; This data has been transferred from InSiGHT LOVDv2 database. - B+; Unknown Lynch Syndrome Additional info: yes; colon (52y); colloid CRC on adenoma; cecum; Pedigree available: yes; MSH6 MSH6 1 1 MAURIZIO GENUARDI
00002452 - - IT - InSiGHT LOVDv2 ID:1013186; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Laura De Lellis
00002473 - ? - - InSiGHT LOVDv2 ID:80; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 2 1 Michael Woods
00002530 - M BR - InSiGHT LOVDv2 ID:1010914; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Felipe Silva
00002559 - ? - - InSiGHT LOVDv2 ID:20846; This data has been transferred from InSiGHT LOVDv2 database. - AII-;B?; - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00002562 Yan et al, 2007 M China - InSiGHT LOVDv2 ID:1013027; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 John Paul Plazzer
00002585 - ? - - InSiGHT LOVDv2 ID:20857; This data has been transferred from InSiGHT LOVDv2 database. - AII-;B?; - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00002643 - ? - - InSiGHT LOVDv2 ID:20875; This data has been transferred from InSiGHT LOVDv2 database. - AII-;B?; - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00002690 Yan et al, 2007 F China - InSiGHT LOVDv2 ID:1013028; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 John Paul Plazzer
00002732 - ? DE - InSiGHT LOVDv2 ID:12685; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Beate Dr. Betz
00002755 - F DE - InSiGHT LOVDv2 ID:1008348; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Martin Digweed
00002809 - ? DE - InSiGHT LOVDv2 ID:12661; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Beate Dr. Betz
00002825 - ? - - InSiGHT LOVDv2 ID:20962; This data has been transferred from InSiGHT LOVDv2 database. - AII-;B?; - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00002836 - F BR - InSiGHT LOVDv2 ID:1010912; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Felipe Silva
00002837 - M BR - InSiGHT LOVDv2 ID:1010919; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Felipe Silva
00002851 - ? DE - InSiGHT LOVDv2 ID:12699; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Beate Dr. Betz
00002867 - ? DE - InSiGHT LOVDv2 ID:12676; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Beate Dr. Betz
00002871 - ? DE - InSiGHT LOVDv2 ID:12689; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Beate Dr. Betz
00002896 - M DE - InSiGHT LOVDv2 ID:1008347; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Martin Digweed
00002908 - - IT - InSiGHT LOVDv2 ID:1013185; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Laura De Lellis
00002937 - - - - InSiGHT LOVDv2 ID:1016807; This data has been transferred from InSiGHT LOVDv2 database. - revised Bethesda; - Lynch Syndrome - MSH6 MSH6 1 1 InSiGHT group
00002967 - F ES Caucasian InSiGHT LOVDv2 ID:1010415; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome Additional info: no Pedigree available: no; MSH6 MSH6 1 1 Javier Garcia-Planells
00002986 - - - - InSiGHT LOVDv2 ID:1016808; This data has been transferred from InSiGHT LOVDv2 database. - revised Bethesda; - Lynch Syndrome - MSH6 MSH6 1 1 InSiGHT group
00002992 - ? - - InSiGHT LOVDv2 ID:25580; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00003024 - ? - - Amsterdam(-)proband's tumor CRC age:57.; InSiGHT LOVDv2 ID:21075; This data has been transferred from InSiGHT LOVDv2 database. - AII-; - Lynch Syndrome located in the (C)8 repetitive region in c termin MSH6 MSH6 1 1 Michael Woods
00003038 - ? - - InSiGHT LOVDv2 ID:25590; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00003047 - - - - InSiGHT LOVDv2 ID:1016809; This data has been transferred from InSiGHT LOVDv2 database. - revised Bethesda; - Lynch Syndrome - MSH6 MSH6 1 1 InSiGHT group
00003048 - - - - InSiGHT LOVDv2 ID:1016810; This data has been transferred from InSiGHT LOVDv2 database. - Amsterdam; - Lynch Syndrome - MSH6 MSH6 1 1 InSiGHT group
00003076 - ? - - reported first by Vasen et al,1991; patient carried missense mutations in both MSH2 and MSH6 but did not fulfil Amsterdam criteria (all affected family members were from one generation); InSiGHT LOVDv2 ID:21101; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00003101 - M MY Malay InSiGHT LOVDv2 ID:1013038; This data has been transferred from InSiGHT LOVDv2 database. - B+; Colorectal symptoms Lynch Syndrome Additional info: transverse colon; MSH6 MSH6 1 1 Mohd Nizam Zahary
00003161 - M BR - InSiGHT LOVDv2 ID:1010936; This data has been transferred from InSiGHT LOVDv2 database. - B+; - Lynch Syndrome - MSH6 MSH6 1 1 Felipe Silva
00003166 - ? - - InSiGHT LOVDv2 ID:25616; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00003180 - ? DE - InSiGHT LOVDv2 ID:12671; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Beate Dr. Betz
00003224 - ? - - the mutation was only identified in the cell line, but not in the patient (according Insight result); ; InSiGHT LOVDv2 ID:21147; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00003282 - M BR - InSiGHT LOVDv2 ID:1010916; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Felipe Silva
00003285 - ? - - InSiGHT LOVDv2 ID:21159; This data has been transferred from InSiGHT LOVDv2 database. - AII-;B?; - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00003341 - ? - - InSiGHT LOVDv2 ID:25606; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00003346 Yan et al, 2007 F China - InSiGHT LOVDv2 ID:1013030; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 John Paul Plazzer
00003349 - F MY Malay InSiGHT LOVDv2 ID:1013032; This data has been transferred from InSiGHT LOVDv2 database. - B+; Colorectal symptoms Lynch Syndrome Additional info: sigmoid colon; MSH6 MSH6 1 1 Mohd Nizam Zahary
00003350 - F BR - InSiGHT LOVDv2 ID:1010918; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Felipe Silva
00003359 - ? - - InSiGHT LOVDv2 ID:25609; This data has been transferred from InSiGHT LOVDv2 database. - - - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
00003375 - ? - - InSiGHT LOVDv2 ID:21191; This data has been transferred from InSiGHT LOVDv2 database. - AII-;B?; - Lynch Syndrome - MSH6 MSH6 1 1 Michael Woods
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