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Terminology chevron_right Concepts chevron_right 1296528004

Production
The component that hold information about this concept.
Cystic fibrosis due to homozygous deltaf508 mutation (disorder)
Deltaf508 homozygous mucoviscidosis
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Cystic fibrosis due to homozygous deltaf508 mutation (disorder)

SCTID: 1296528004, Primitive, Active


1296528004|Cystic fibrosis due to homozygous deltaf508 mutation (disorder)|
  • en Cystic fibrosis due to homozygous deltaf508 mutation
  • en Cystic fibrosis due to homozygous deltaf508 mutation (disorder)
  • en Deltaf508 homozygous cystic fibrosis
  • en Deltaf508 homozygous mucoviscidosis

1296528004 |Cystic fibrosis due to homozygous deltaf508 mutation (disorder)|

<<< 190905008 |Cystic fibrosis (disorder)| :
        { 363713009 |Has interpretation (attribute)| = 260379002 |Impaired (qualifier value)|,
          363714003 |Interprets (attribute)| = 63533009 |Mucociliary clearance, function (observable entity)| }
        { 363698007 |Finding site (attribute)| = 321667001 |Respiratory tract structure (body structure)| }
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