C0005283 - An autosomal recessive disorder that affects the production of beta polypeptide chains that are necessary for hemoglobin synthesis. Anemia and failure to thrive are characteristic features. 1/10
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Terms, descriptions
CUI    C0005283
RussianMedical Subject Headings Russian D017086 L3341123preferred S3868616 Y БЕТА-ТАЛАССЕМИЯ
RussianMedical Subject Headings Russian D017086 L0891139no S1094956 Y BETA-TALASSEMIIA
RussianMedical Subject Headings Russian D017086 L1508529no S1804438 Y ANEMIIA ERITROBLASTICHESKAIA
RussianMedical Subject Headings Russian D017086 L1508536no S1804445 Y ANEMIIA KULI
RussianMedical Subject Headings Russian D017086 L1508544no S1804453 Y ANEMIIA SREDIZEMNOMORSKAIA
RussianMedical Subject Headings Russian D017086 L1521083no S1816992 Y GEMOGLOBINOPATIIA F
RussianMedical Subject Headings Russian D017086 L1544939no S1840848 Y TALASSEMIIA BETA
RussianMedical Subject Headings Russian D017086 L1544940no S1840849 Y TALASSEMIIA BOL'SHAIA
RussianMedical Subject Headings Russian D017086 L1544941no S1840850 Y TALASSEMIIA MALAIA
RussianMDRRUS 10004505 L15722285no S19020345 Y Бета-талассемия
RussianMDRRUS 10043391 L15752615no S19084815 N Талассемия-бета
RussianMDRRUS 10043391 L15752615no S19084815 Y Талассемия-бета
RussianMDRRUS 10004514 L15766625no S19020341 Y Бета талассемия
RussianMDRRUS 10054660 L15785607no S19084804 Y Талассемия бета
RussianMedical Subject Headings Russian D017086 L3338506no S3865987 Y АНЕМИЯ КУЛИ
RussianMedical Subject Headings Russian D017086 L3338522no S3866003 Y АНЕМИЯ СРЕДИЗЕМНОМОРСКАЯ
RussianMedical Subject Headings Russian D017086 L3338525no S3866006 Y АНЕМИЯ ЭРИТРОБЛАСТИЧЕСКАЯ
RussianMedical Subject Headings Russian D017086 L3344084no S3871558 Y ГЕМОГЛОБИНОПАТИЯ F
RussianMedical Subject Headings Russian D017086 L3371367no S3898860 Y ТАЛАССЕМИЯ БЕТА
RussianMedical Subject Headings Russian D017086 L3371368no S3898861 Y ТАЛАССЕМИЯ БОЛЬШАЯ
RussianMedical Subject Headings Russian D017086 L3371369no S3898862 Y ТАЛАССЕМИЯ МАЛАЯ
Medical Subject Headings A0030415 AT38151155 A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent.
MSHNOR A24286773 AT221521778 En sykdom karakterisert ved redusert syntese av betakjeder i hemoglobin. Resultatet er forsinkelse i syntesen av hemoglobin A ved den heterozygote tilstanden (thalassemia minor) som er asymptomatisk, mens den homozygote tilstanden (thalassemia major, Cooleys anemi, Middelhavsanemi, erytroblastisk anemi) er forbundet med alvorlige komplikasjoner og også død. Her syntetiseres det ikke hemoglobin A.
NCI Thesaurus A27934466 AT198054447 An autosomal recessive disorder that affects the production of beta polypeptide chains which are necessary for the hemoglobin synthesis. Anemia and failure to thrive are characteristic features.
NCI National Institute of Child Health and Human Development A27934466 AT224195030 An autosomal recessive disorder that affects the production of beta polypeptide chains that are necessary for hemoglobin synthesis. Anemia and failure to thrive are characteristic features.