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The way concept relations are shown:
alpha-Thalassemia
Hierarchy: | ∟ ∟ ∟ ∟ ∟ alpha-Thalassemia 1 coordinate concept1 subordinate concept∟ ∟ ∟ ∟ ∟ alpha-Thalassemia 1 coordinate concept1 subordinate concept∟ ∟ ∟ ∟ ∟ ∟ ∟ alpha-Thalassemia 1 coordinate concept1 subordinate concept∟ ∟ ∟ ∟ ∟ alpha-Thalassemia 1 coordinate concept1 subordinate conceptX |
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Annotation: | do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
X |
History note: | Thalassemia (1966-1992)X |
historyNote*: | 93; was see THALASSEMIA 1988-92; HEMOGLOBIN H DISEASE was see THALASSEMIA 1982-92
X |
onlineNote*: | use THALASSEMIA to search ALPHA-THALASSEMIA 1988-92 & HEMOGLOBIN H DISEASE 1982-92
X |
publicMeSHNote*: | 93; was see THALASSEMIA 1988-92; HEMOGLOBIN H DISEASE was see THALASSEMIA 1982-92
X |
Scope note: | 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.
X |
activeMeSHYear*: | |
dateCreated*: | 1992-05-07X |
dateEstablished*: | 1993-01-01X |
dateRevised*: | 2001-07-25X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | nnsX |
recordOriginator*: | PXPX |
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Labels and equivalent concepts: | Alfatalassemia (fi) XAlfatalassemi (sv) Thalassemia-alpha (en, replaced) Hemoglobin H Disease (en, replaced) Thalassaemia alpha (la-FI, replaced) |
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