137
edits
Changes
Myeloid Neoplasms with Germline Predisposition (view source)
Revision as of 14:54, 1 March 2021
, 14:54, 1 March 2021no edit summary
==Other Related Pages (Includes Links to Content)==
==Other Related Pages (Includes Links to Content)==
NA
==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])