Disease #00005 (HNPCC (Lynch syndrome), OMIM:609309)

Official abbreviation HNPCC
Name Lynch syndrome
OMIM ID 609309
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 7
Phenotype entries for this disease 1
Associated with 3 genes MSH2, MSX1, PMS2
Associated tissues colon
Disease features -
Remarks -


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00000005 MN Zahary et al. (2012) - - - - - - HNPCC - MSH2 MSH2 1 1 MyHVP
00000416 Wan Juhari, W. K(2020) M Malaysia Malay - - - HNPCC - MLH1 MLH1 1 1 Nur Aisyah Athirah
00000417 Wan Juhari, W. K.(2020) F Malaysia Malay - - - HNPCC - MSH2 MSH2 4 2 Nur Aisyah Athirah
00000418 Wan Juhari, W. K.(2020) F Malaysia Malay - - - HNPCC - MSH2 MSH2 1 1 Nur Aisyah Athirah
00000419 Wan Juhari, W. K.(2020) M Malaysia Malay - - - HNPCC - MLH1 MLH1 1 1 Nur Aisyah Athirah
00000420 Wan Juhari, W. K.(2020) F Malaysia Malay - - - HNPCC - MLH1, MSH2 MLH1, MSH2 4 2 Nur Aisyah Athirah
00000421 Wan Juhari, W. K.(2020) F Malaysia Malay - - - HNPCC - MLH1, MSH2 MLH1, MSH2 3 1 Nur Aisyah Athirah
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