SNOMED CT

Last uploaded: January 16, 2025
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Id http://purl.bioontology.org/ontology/SNOMEDCT/16360009
http://purl.bioontology.org/ontology/SNOMEDCT/16360009
Preferred Name

Delta beta thalassemia
Synonyms
F thalassemia
Delta beta thalassaemia
F thalassaemia
Delta beta thalassemia (disorder)
Delta-beta thalassemia
Delta-beta thalassaemia
Type http://www.w3.org/2002/07/owl#Class

All Properties

altLabel
F thalassemia
Delta beta thalassaemia
F thalassaemia
Delta beta thalassemia (disorder)
Delta-beta thalassemia
Delta-beta thalassaemia
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prefLabel
Delta beta thalassemia
Type ID
900000000000003001
900000000000013009
CASE SIGNIFICANCE ID
900000000000020002
900000000000448009
900000000000017005
notation
16360009
Effective time
20020131
Active
1
Has finding site
INACTIVATION INDICATOR
723277005
interprets
subClassOf
Semantic type UMLS property
Has interpretation
type
Subset member
447562003~MAPRULE~TRUE
6011000124106~MAPRULE~IFA 127044007 | Sickle cell-delta beta^0^-thalassemia (disorder) |
900000000000490003~VALUEID~723277005
6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
6011000124106~MAPADVICE~IF HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN DELTA BETA PLUS THALASSEMIA CHOOSE D56.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~
6011000124106~MAPCATEGORYID~447638001
6011000124106~MAPADVICE~IF HPFH DELTA BETA^0^ THALASSEMIA CHOOSE D56.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
6011000124106~MAPTARGET~D56.4
447562003~MAPADVICE~ALWAYS D56.2
6011000124106~MAPRULE~IFA 54006005 | HPFH delta beta^0^ thalassemia |
6011000124106~MAPRULE~IFA 54006005 | Hereditary persistence of fetal hemoglobin delta beta^0^ thalassemia (disorder) |
900000000000508004~ACCEPTABILITYID~900000000000549004
6011000124106~MAPTARGET~D57.40
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPTARGET~D57.3
6011000124106~MAPADVICE~ALWAYS D56.2
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPTARGET~D56.2
6011000124106~MAPRULE~IFA 54006005 | Hereditary persistence of fetal hemoglobin delta beta plus thalassemia |
900000000000508004~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~IF SICKLE CELL-DELTA BETA^0^-THALASSEMIA CHOOSE D57.3 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
447562003~MAPTARGET~D56.2
6011000124106~MAPRULE~OTHERWISE TRUE
900000000000497000~MAPTARGET~X20Cq
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPADVICE~IF SICKLE CELL-DELTA BETA^0^-THALASSEMIA CHOOSE D57.40 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
6011000124106~MAPADVICE~IF SICKLE CELL-DELTA BETA^0^-THALASSEMIA CHOOSE D56.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 127044007 | Sickle cell-delta beta^0^-thalassemia |
6011000124106~MAPADVICE~IF HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN DELTA BETA^0^ THALASSEMIA CHOOSE D56.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~3
900000000000509007~ACCEPTABILITYID~900000000000549004
6011000124106~MAPPRIORITY~2
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DEFINITION STATUS ID
900000000000074008
tui
T047
CTV3ID
X20Cq
Occurs in
cui
C0271985
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