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Familial myelofibrosis

MedGen UID:
444034
•Concept ID:
C2931351
•
Disease or Syndrome
Synonym: familial myelofibrosis
 
Monarch Initiative: MONDO:0023119

Professional guidelines

PubMed

A TET2 rs3733609 C/T genotype is associated with predisposition to the myeloproliferative neoplasms harboring JAK2(V617F) and confers a proliferative potential on erythroid lineages.
Shen XH, Sun NN, Yin YF, Liu SF, Liu XL, Peng HL, Dai CW, Xu YX, Deng MY, Luo YY, Zheng WL, Zhang GS
Oncotarget 2016 Feb 23;7(8):9550-60. doi: 10.18632/oncotarget.7072. PMID: 26843622Free PMC Article

Curated

NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®), Myeloproliferative Neoplasms, 2023

Recent clinical studies

Etiology

A TET2 rs3733609 C/T genotype is associated with predisposition to the myeloproliferative neoplasms harboring JAK2(V617F) and confers a proliferative potential on erythroid lineages.
Shen XH, Sun NN, Yin YF, Liu SF, Liu XL, Peng HL, Dai CW, Xu YX, Deng MY, Luo YY, Zheng WL, Zhang GS
Oncotarget 2016 Feb 23;7(8):9550-60. doi: 10.18632/oncotarget.7072. PMID: 26843622Free PMC Article

Diagnosis

Familial myelofibrosis.
Sieff CA, Malleson P
Arch Dis Child 1980 Nov;55(11):888-93. doi: 10.1136/adc.55.11.888. PMID: 7436463Free PMC Article

Supplemental Content

Table of contents

    Clinical resources

    Practice guidelines

    • PubMed
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    Curated

    • NCCN, 2023
      NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®), Myeloproliferative Neoplasms, 2023

    Reviews

    Related information

    • ClinVar
      Related medical variations
    • MeSH
      Related Medical Subject Headings
    • PMC Articles
      Related information in PubMed Central Links
    • PubMed
      Related literature resources in PubMed

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