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Terminology chevron_right Concepts chevron_right 127045008

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The component that hold information about this concept.
Sickle cell anemia with coexistent alpha-thalassemia (disorder)
Sickle cell anemia with coexistent alpha-thalassemia
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Sickle cell anemia with coexistent alpha-thalassemia (disorder)

SCTID: 127045008, Primitive, Active


127045008|Sickle cell anemia with coexistent alpha-thalassemia (disorder)|
  • en Sickle cell anaemia with coexistent alpha-thalassaemia
  • en Sickle cell anemia with coexistent alpha-thalassemia
  • en Sickle cell anemia with coexistent alpha-thalassemia (disorder)

127045008 |Sickle cell anemia with coexistent alpha-thalassemia (disorder)|

<<< 68913001 |Alpha thalassemia (disorder)| +
    36472007 |Sickle cell-thalassemia disease (disorder)| +
    127040003 |Hereditary hemoglobinopathy disorder homozygous for hemoglobin s (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 49938009 |Drepanocyte (cell)|,
          363698007 |Finding site (attribute)| = 57171008 |Hematopoietic system structure (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
          363714003 |Interprets (attribute)| = 441689006 |Measurement of total hemoglobin concentration (procedure)| }
        { 363698007 |Finding site (attribute)| = 41898006 |Erythrocyte (cell)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 246075003 |Causative agent (attribute)| = 50095005 |Hemoglobin s (substance)| }
Active
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