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Terminology chevron_right Concepts chevron_right 27798002

Production
The component that hold information about this concept.
Megaloblastic anemia due to impaired absorption of folate (disorder)
Congenital folate malabsorption
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Megaloblastic anemia due to impaired absorption of folate (disorder)

SCTID: 27798002, Primitive, Active


27798002|Megaloblastic anemia due to impaired absorption of folate (disorder)|
  • en Megaloblastic anaemia due to impaired absorption of folate
  • en Megaloblastic anemia due to impaired absorption of folate
  • en Megaloblastic anemia due to impaired absorption of folate (disorder)

27798002 |Megaloblastic anemia due to impaired absorption of folate (disorder)|

<<< 85649008 |Megaloblastic anemia due to folate deficiency (disorder)| +
    165397008 |Hemoglobin below reference range (finding)| +
    165423001 |Red blood cell count below reference range (finding)| :
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
          363714003 |Interprets (attribute)| = 441689006 |Measurement of total hemoglobin concentration (procedure)| }
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
          363714003 |Interprets (attribute)| = 14089001 |Red blood cell count (procedure)| }
        { 42752001 |Due to (attribute)| = 190633005 |Folic acid deficiency (disorder)| }
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