| Descriptor English: | GATA2 Deficiency | ||||||
| Descriptor Spanish: |
Deficiencia GATA2
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| 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 |
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| Tree number(s): |
C15.378.190.625.265 C16.320.314 |
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| 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. |
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| 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 |
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| Previous Indexing: |
GATA2 Transcription Factor (2011-2018) |
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| Public MeSH Note: | 2019 |
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| History Note: | 2019 |
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| 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 |
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GATA2 Deficiency
- Preferred
Natural Killer Cell Deficiency
- Related but not broader or narrower
Emberger Syndrome
- Related but not broader or narrower
Myelodysplastic Syndrome Acute Myeloid Leukemia
- Related but not broader or narrower
| 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 |
| Concept UI |
M000640868 |
| Preferred term | Natural Killer Cell Deficiency |
| Concept UI |
M000640869 |
| Preferred term | Emberger Syndrome |
| Entry term(s) |
Primary Lymphedema with Myelodysplasia |
| Concept UI |
M000641166 |
| Preferred term | Myelodysplastic Syndrome Acute Myeloid Leukemia |
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