Changes

Johns Hopkins University, Baltimore, MD  

Johns Hopkins University, Baltimore, MD  

==General Disease Overview / Description of Cancer Category==

==General Disease Overview / Description of Cancer Category==

==WHO Classification Pages (Includes Links to Content)==

==WHO Classification Pages (Includes Links to Content)==

*[[Acute Myeloid Leukaemia with Germline CEBPA Mutation]]

*[[HAEM4:Acute Myeloid Leukaemia with Germline CEBPA Mutation]]

*[[Myeloid Neoplasms with Germline DDX41 Mutation]]

*[[HAEM4:Myeloid Neoplasms with Germline DDX41 Mutation]]

*[[Myeloid Neoplasms with Germline RUNX1 Mutation]]

*[[HAEM4:Myeloid Neoplasms with Germline RUNX1 Mutation]]

*[[Myeloid Neoplasms with Germline ANKRD26 Mutation]]

*[[HAEM4:Myeloid Neoplasms with Germline ANKRD26 Mutation]]

*[[Myeloid Neoplasms with Germline ETV6 Mutation]]

*[[HAEM4:Myeloid Neoplasms with Germline ETV6 Mutation]]

*[[Myeloid Neoplasms with Germline GATA2 Mutation]]

*[[HAEM4:Myeloid Neoplasms with Germline GATA2 Mutation]]

==Other Related Pages (Includes Links to Content)==

==Other Related Pages (Includes Links to Content)==

==Additional Information==

==Additional Information==

*TP53 (OMIM: [https://omim.org/entry/191170 191170]) has been associated with Li-Fraumeni syndrome (OMIM: [https://www.omim.org/entry/151623 151623])

*TP53 (OMIM: [https://omim.org/entry/191170 191170]) has been associated with Li-Fraumeni syndrome (OMIM: [https://www.omim.org/entry/151623 151623])

*BLM (OMIM: [https://omim.org/entry/604610 604610]) has been associated with Bloom syndrome (OMIM: [https://www.omim.org/entry/210900 210900])

*BLM (OMIM: [https://omim.org/entry/604610 604610]) has been associated with Bloom syndrome (OMIM: [https://www.omim.org/entry/210900 210900])

*Constitutional mismatch repair deficiency (OMIM: [https://www.omim.org/entry/276300 276300])  

*Constitutional mismatch repair deficiency (OMIM: [https://www.omim.org/entry/276300 276300])

*Neurofibromatosis type I (NF1, OMIM: [https://www.omim.org/entry/162200 162200])

*Neurofibromatosis type I (NF1, OMIM: [https://www.omim.org/entry/162200 162200])

*Nijmegen breakage syndrome (NBS, OMIM: [https://www.omim.org/entry/251260 251260])  

*Nijmegen breakage syndrome (NBS, OMIM: [https://www.omim.org/entry/251260 251260])

*Noonan syndrome (please see Genetic heterogeneity of Noonan syndrome at OMIM: [https://www.omim.org/entry/163950 163950])

*Noonan syndrome (please see Genetic heterogeneity of Noonan syndrome at OMIM: [https://www.omim.org/entry/163950 163950])

*Fanconi anemia (FA, please see Genetic heterogeneity of Fanconi anemia at OMIM: [https://www.omim.org/entry/227650 227650])  

*Fanconi anemia (FA, please see Genetic heterogeneity of Fanconi anemia at OMIM: [https://www.omim.org/entry/227650 227650])

*Dyskeratosis congenital (DC, please see Genetic heterogeneity of dyskeratosis congenital at OMIM: [https://www.omim.org/entry/127550 127550])  

*Dyskeratosis congenital (DC, please see Genetic heterogeneity of dyskeratosis congenital at OMIM: [https://www.omim.org/entry/127550 127550])

*Severe congenital neutropenia (SCN, please see Genetic heterogeneity of severe congenital neutropenia at OMIM; [https://www.omim.org/entry/202700 202700])  

*Severe congenital neutropenia (SCN, please see Genetic heterogeneity of severe congenital neutropenia at OMIM; [https://www.omim.org/entry/202700 202700])

*Shwachman-Diamond syndrome 1 (SDS1, OMIM: [https://www.omim.org/entry/260400 260400]) and Shwachman-Diamond syndrome 2 (SDS2, OMIM: [https://www.omim.org/entry/617941 617941])

*Shwachman-Diamond syndrome 1 (SDS1, OMIM: [https://www.omim.org/entry/260400 260400]) and Shwachman-Diamond syndrome 2 (SDS2, OMIM: [https://www.omim.org/entry/617941 617941])

*Diamond Blackfan anemia (DBA, please see Genetic heterogeneity of Diamond Blackfan anemia at OMIM: [https://www.omim.org/entry/105650 105650])

*Diamond Blackfan anemia (DBA, please see Genetic heterogeneity of Diamond Blackfan anemia at OMIM: [https://www.omim.org/entry/105650 105650])

<nowiki>*</nowiki>Primary authors will typically be those that initially create and complete the content of a page.  If a subsequent user modifies the content and feels the effort put forth is of high enough significance to warrant listing in the authorship section, please contact the CCGA coordinators (contact information provided on the homepage).  Additional global feedback or concerns are also welcome.

<nowiki>*</nowiki>Primary authors will typically be those that initially create and complete the content of a page.  If a subsequent user modifies the content and feels the effort put forth is of high enough significance to warrant listing in the authorship section, please contact the CCGA coordinators (contact information provided on the homepage).  Additional global feedback or concerns are also welcome.

[[Category:Diseases M]]

<nowiki>*</nowiki>The hierarchical tumour classification structure displayed on this page is reproduced from the [https://tumourclassification.iarc.who.int/welcome/ WHO Classification of Tumours] with permission from the copyright holder, ©International Agency for Research on Cancer.

 

 

[[Category:Oncogenes in AML]]

[[Category:Oncogenes in AML]]

[[Category:Cancer Genes A]]

[[Category:Cancer Genes A]]

[[Category:Cancer Genes E]]

[[Category:Cancer Genes E]]

[[Category:Cancer Genes G]]

[[Category:Cancer Genes G]]

[[Category:Cancer Genes R]]

[[Category:Cancer Genes R]]

[[Category:Recently Added Pages]]

[[Category:Recently Added Pages]]