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 C0002881 | |||||||
Russian | Medical Subject Headings Russian | D000745 | L3338492 | preferred | S3865973 | Y | АНЕМИЯ ГЕМОЛИТИЧЕСКАЯ ВРОЖДЕННАЯ |
Russian | Medical Subject Headings Russian | D000745 | L0889990 | no | S1093807 | Y | ANEMIIA GEMOLITICHESKAIA VROZHDENNAIA |
Russian | MDRRUS | 10019880 | L15714968 | no | S19049477 | Y | Наследственная гемолитическая анемия, БДУ |
Russian | MDRRUS | 10073793 | L15722787 | no | S19024494 | Y | Врожденная гемолитическая анемия |
Russian | MDRRUS | 10010489 | L15756115 | no | S19024493 | Y | Врожденная гемолитическая анемия, БДУ |
Russian | MDRRUS | 10019881 | L15759235 | no | S19049478 | Y | Наследственная гемолитическая анемия, неуточненная |
Russian | MDRRUS | 10019885 | L15767398 | no | S19026736 | Y | Гемолитическая анемия, наследственная, неуточненная |
Russian | MDRRUS | 10060893 | L15770253 | no | S19049479 | N | Наследственная гемолитическая анемия |
Russian | MDRRUS | 10060893 | L15770253 | no | S19049479 | Y | Наследственная гемолитическая анемия |
Russian | MDRRUS | 10055202 | L15778191 | no | S19025110 | Y | Врождённая гемолитическая анемия |
Russian | MDRRUS | 10054399 | L15789278 | no | S19026737 | Y | Гемолитическая анемия, наследственная |
Russian | MDRRUS | 10019886 | L15789287 | no | S19026791 | Y | Гемолитические анемии, наследственные |
Russian | MDRRUS | 10019882 | L15792099 | no | S19049520 | Y | Наследственные гемолитические анемии |
Russian | Medical Subject Headings Russian | D000745 | L2226794 | no | S2565016 | Y | ANEMIIA GEMOLITICHESKAIA NASLEDSTVENNAIA |
Russian | Medical Subject Headings Russian | D000745 | L3338496 | no | S3865977 | Y | АНЕМИЯ ГЕМОЛИТИЧЕСКАЯ НАСЛЕДСТВЕННАЯ |
Medical Subject Headings | A0023691 | AT38133032 | Hemolytic anemia due to various intrinsic defects of the erythrocyte. | ||||
(CPTSP) CRISP Thesaurus | A0476623 | AT51219211 | includes hereditary erythrocyte membrane defects, enzyme deficiencies, hemoglobin abnormalities, stem cell defects (paroxysmal nocturnal hemoglobinuria), and alloimmune (Rh) disease of newborn. | ||||
HPO | A24668992 | AT206301900 | A form of hemolytic anemia with congenital onset. [HPO:probinson] | ||||
NCI Thesaurus | A7582790 | AT198042187 | A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies. | ||||
NCI National Institute of Child Health and Human Development | A7582790 | AT224183621 | Hemolytic anemia for which the cause is an inherited disorder. |