Alpha thalassaemia myelodysplastic syndrome (Q91736): Difference between revisions
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Talassemia alfa é um tipo de talassemia envolvendo os genes HBA1 e HBA2. A talassemia alfa é devida a produção prejudicada das cadeias da alfa globina 1,2,3 ou 4, levando a um excesso relativo de cadeias da beta globina. A síndrome mielodisplásica é uma coleção diversa de condições médicas hematológicas (relacionadas ao sangue) que envolve produção ineficaz (ou displasia) de células sanguíneas da classe mieloides. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Alpha-thalassemia is a form of thalassemia involving the genes HBA1 and HBA2. Alpha-thalassemia is due to impaired production of 1,2,3, or 4 alpha globin chains, leading to a relative excess of beta globin chains. Myelodysplastic syndrome is a diverse collection of haematological (blood-related) medical conditions that involve ineffective production (or dysplasia) of the myeloid class of blood cells. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1991581630 / rank | |||||||||||||||
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CID11:ID_1991581630 | |||||||||||||||
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dki-india-ID_1991581630 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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Latest revision as of 18:46, 15 August 2026
Alpha-thalassemia is a form of thalassemia involving the genes HBA1 and HBA2. Alpha-thalassemia is due to impaired production of 1,2,3, or 4 alpha globin chains, leading to a relative excess of beta globin chains. Myelodysplastic syndrome is a diverse collection of haematological (blood-related) medical conditions that involve ineffective production (or dysplasia) of the myeloid class of blood cells.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1991581630 |
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| English | Alpha thalassaemia myelodysplastic syndrome |
Alpha-thalassemia is a form of thalassemia involving the genes HBA1 and HBA2. Alpha-thalassemia is due to impaired production of 1,2,3, or 4 alpha globin chains, leading to a relative excess of beta globin chains. Myelodysplastic syndrome is a diverse collection of haematological (blood-related) medical conditions that involve ineffective production (or dysplasia) of the myeloid class of blood cells. |
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CID11:ID_1991581630
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dki-india-ID_1991581630
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Concluído
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13 August 2026
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