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Concept information

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > GATA2 Deficiency
Hemic and Lymphatic Diseases > Hematologic Diseases > Bone Marrow Diseases > Myelodysplastic Syndromes > GATA2 Deficiency

Preferred term

GATA2 Deficiency  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • GATA2 Haploinsufficiencies
  • GATA2 Haploinsufficiency
  • Immunodeficiency type 21
  • MonoMac Syndrome
  • MonoMac Syndromes

Scope note

  • A rare disorder of the immune system with wide-ranging effects which include GATA2 Transcription Factor dysfunction, immunodeficiency, myelodysplastic syndrome (ineffective blood cell production), lung disease, and problems of the vascular and lymphatic system.

History note

  • 2019

In other languages

  • GATA2:n puute

    Finnish

  • GATA2:n puutos
  • GATA2-brist

    Swedish

  • Embergers syndrom
  • Myelodysplastiskt syndrom/Akut myeloisk leukemi
  • NK-cell brist

URI

http://www.yso.fi/onto/mesh/D000077428

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