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Hemoglobinopathies
Hierarchy: | ∟ ∟ ∟ Hemoglobinopathies 50 coordinate concepts3 subordinate concepts∟ Anemia | ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ CADASIL | ∟ ∟ ∟ ∟ ∟ ∟ Dwarfism | ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hemoglobinopathies 50 coordinate concepts3 subordinate concepts∟ Anemia | ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ CADASIL | ∟ ∟ ∟ ∟ ∟ ∟ Dwarfism | ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
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Annotation: | do not confuse with HEMOGLOBINS, ABNORMAL (D12): use term in the text; coord IM with specific abnormal hemoglobin (IM) but HEMOGLOBIN C DISEASE; THALASSEMIA (hemoglobin H disease) & ANEMIA, SICKLE CELL (hemoglobin S disease) are available
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historyNote*: | 68
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publicMeSHNote*: | 68
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Scope note: | A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.
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activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1968-01-01X |
dateRevised*: | 2001-07-25X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | nnsX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Hemoglobinopatiat (fi) XVerenpunataudit (fi, replaced) Verenpunasairaudet (fi, replaced) Hemoglobiinitaudit (fi, replaced) Hemoglobinopatia (fi, replaced) Hemoglobiinisairaudet (fi, replaced) Hemoglobinopatier (sv) Hemoglobinsjukdomar (sv, replaced) Haemoglobinopathia (la-FI, replaced) |
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