137
edits
Changes
Myeloid Neoplasms with Germline Predisposition (view source)
Revision as of 12:03, 19 January 2021
, 12:03, 19 January 2021→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: 276300) , <nowiki>https://www.omim.org/entry/276300</nowiki>)
*Constitutional mismatch repair deficiency (OMIM: [https://www.omim.org/entry/276300 276300])
*Neurofibromatosis type I (NF1, OMIM: 162200) , <nowiki>https://www.omim.org/entry/162200</nowiki>)
*Neurofibromatosis type I (NF1, OMIM: [https://www.omim.org/entry/162200 162200])
*Nijmegen breakage syndrome (NBS, OMIM: 251260) , <nowiki>https://www.omim.org/entry/251260</nowiki>)
*Nijmegen breakage syndrome (NBS, OMIM: [https://www.omim.org/entry/251260 251260])
*Noonan syndrome (please see Genetic heterogeneity of Noonan syndrome at OMIM: 163950) <nowiki>https://www.omim.org/entry/163950</nowiki>
*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: 227650) <nowiki>https://www.omim.org/entry/227650</nowiki>),
*Fanconi anemia (FA, please see Genetic heterogeneity of Fanconi anemia at OMIM: 227650) <nowiki>https://www.omim.org/entry/227650</nowiki>),
*Dyskeratosis congenital (DC, please see Genetic heterogeneity of dyskeratosis congenital at OMIM: 127550) <nowiki>https://www.omim.org/entry/127550</nowiki>).
*Dyskeratosis congenital (DC, please see Genetic heterogeneity of dyskeratosis congenital at OMIM: 127550) <nowiki>https://www.omim.org/entry/127550</nowiki>).