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Descriptor English: GATA2 Deficiency
Descriptor Spanish: Deficiencia GATA2
Descriptor Portuguese: Deficiência de GATA2
Descriptor French: Déficience en GATA2
Entry term(s): Emberger Syndrome
GATA2 Deficiencies
GATA2 Haploinsufficiencies
GATA2 Haploinsufficiency
Immunodeficiency type 21
MonoMac Syndrome
MonoMac Syndromes
Myelodysplastic Syndrome Acute Myeloid Leukemia
Natural Killer Cell Deficiency
Primary Lymphedema with Myelodysplasia
Tree number(s): C15.378.190.625.265
C16.320.314
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D000077428
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.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DF deficiency
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: GATA2 Transcription Factor (2011-2018)
Public MeSH Note: 2019
History Note: 2019
DeCS ID: 57644
Unique ID: D000077428
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2019/01/01
Date of Entry: 2018/07/09
Revision Date: 2018/06/14
GATA2 Deficiency - Preferred
Concept UI M000640742
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.
Preferred term GATA2 Deficiency
Entry term(s) GATA2 Deficiencies
GATA2 Haploinsufficiencies
GATA2 Haploinsufficiency
Immunodeficiency type 21
MonoMac Syndrome
MonoMac Syndromes
Natural Killer Cell Deficiency - Related but not broader or narrower
Concept UI M000640868
Preferred term Natural Killer Cell Deficiency
Emberger Syndrome - Related but not broader or narrower
Concept UI M000640869
Preferred term Emberger Syndrome
Entry term(s) Primary Lymphedema with Myelodysplasia
Myelodysplastic Syndrome Acute Myeloid Leukemia - Related but not broader or narrower
Concept UI M000641166
Preferred term Myelodysplastic Syndrome Acute Myeloid Leukemia



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