293,031 терминов и синонимов из MeSH и LOINC
Lang Dictionary CODE | LUI | preferred no |
SUI | preference Yes / No |
Terms, descriptions |
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CUI C0002312 | |||||||
Russian | Medical Subject Headings Russian | D017085 | L3337846 | preferred | S3865336 | Y | АЛЬФА-ТАЛАССЕМИЯ |
Russian | Medical Subject Headings Russian | D017085 | L0889672 | no | S1093489 | Y | AL'FA-TALASSEMIIA |
Russian | Medical Subject Headings Russian | D017085 | L1521084 | no | S1816993 | Y | GEMOGLOBINOPATIIA H |
Russian | Medical Subject Headings Russian | D017085 | L1544938 | no | S1840847 | Y | TALASSEMIIA AL'FA |
Russian | MDRRUS | 10054659 | L15719359 | no | S19084803 | Y | Талассемия альфа |
Russian | MDRRUS | 10043390 | L15741482 | no | S19084814 | N | Талассемия-альфа |
Russian | MDRRUS | 10043390 | L15741482 | no | S19084814 | Y | Талассемия-альфа |
Russian | MDRRUS | 10001817 | L15766178 | no | S19016793 | Y | Альфа талассемия |
Russian | MDRRUS | 10001802 | L15777114 | no | S19016804 | Y | Альфа-талассемия |
Russian | Medical Subject Headings Russian | D017085 | L3344085 | no | S3871559 | Y | ГЕМОГЛОБИНОПАТИЯ H |
Russian | Medical Subject Headings Russian | D017085 | L3371366 | no | 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. |