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Terminology chevron_right Concepts chevron_right 307115002

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307115002
The component that hold information about this concept.
Homozygous factor v leiden mutation (disorder)
Homozygous factor v leiden mutation
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Homozygous factor v leiden mutation (disorder)

SCTID: 307115002, Primitive, Active


307115002|Homozygous factor v leiden mutation (disorder)|
  • vi Đột biến yếu tố v leiden đồng hợp tử
  • en Homozygous factor v leiden mutation
  • en Homozygous factor v leiden mutation (disorder)

307115002 |Homozygous factor v leiden mutation (disorder)|

<<< 307091009 |Factor v leiden mutation (disorder)| :
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
          363714003 |Interprets (attribute)| = 74848003 |Hemostatic function (observable entity)| }
Active

591061000003110 - đột biến yếu tố V Leiden đồng hợp tử (vi) View

591061000003110
vi
Synonym (core metadata concept)
đột biến yếu tố V Leiden đồng hợp tử
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

450295015 - Homozygous Factor V Leiden mutation (en) View

450295015
en
Synonym (core metadata concept)
Homozygous Factor V Leiden mutation
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

703597014 - Homozygous Factor V Leiden mutation (disorder) (en) View

703597014
en
Fully specified name (core metadata concept)
Homozygous Factor V Leiden mutation (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

307091009 View

307091009
Factor v leiden mutation (disorder)
Đột biến yếu tố v leiden
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True
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