C0002312 - A genetic hematologic disorder characterized by loss of function mutations in one or more of the alpha globin genes. 1/10
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Terms, descriptions
CUI    C0002312
RussianMedical Subject Headings Russian D017085 L3337846preferred S3865336 Y АЛЬФА-ТАЛАССЕМИЯ
RussianMedical Subject Headings Russian D017085 L0889672no S1093489 Y AL'FA-TALASSEMIIA
RussianMedical Subject Headings Russian D017085 L1521084no S1816993 Y GEMOGLOBINOPATIIA H
RussianMedical Subject Headings Russian D017085 L1544938no S1840847 Y TALASSEMIIA AL'FA
RussianMDRRUS 10054659 L15719359no S19084803 Y Талассемия альфа
RussianMDRRUS 10043390 L15741482no S19084814 N Талассемия-альфа
RussianMDRRUS 10043390 L15741482no S19084814 Y Талассемия-альфа
RussianMDRRUS 10001817 L15766178no S19016793 Y Альфа талассемия
RussianMDRRUS 10001802 L15777114no S19016804 Y Альфа-талассемия
RussianMedical Subject Headings Russian D017085 L3344085no S3871559 Y ГЕМОГЛОБИНОПАТИЯ H
RussianMedical Subject Headings Russian D017085 L3371366no S3898859 Y ТАЛАССЕМИЯ АЛЬФА
Medical Subject Headings A0022151 AT38139257 A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted.
Medical Subject Headings Czech A27594962 AT195260505 Porucha alfa-řetězců. Podle počtu fungujících genů pro alfa-řetězec (normálně celkem dva páry, čili čtyři geny) existují formy s různou závažností. Nejzávažnější je mutace všech čtyř genů s výskytem hemoglobinu Bart, která je neslučitelná se životem. (cit. Velký lékařský slovník online, 2013 http://lekarske.slovniky.cz/ )
NCI Thesaurus A7604926 AT198078935 A genetic hematologic disorder characterized by partial or complete absence of the alpha globin chains of the heme molecule.
NCI National Institute of Child Health and Human Development A7604926 AT224187041 A genetic hematologic disorder characterized by loss of function mutations in one or more of the alpha globin genes.