Loading...
dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 726051002

Production
add
  • Extended Map with ID “e36790cd-e014-571d-a7ce-98d4065ce199” doesn’t exist. Perhaps it was deleted?
726051002
The component that hold information about this concept.
Myotonia congenita (disorder)
Myotonia congenita
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

Myotonia congenita (disorder)

SCTID: 726051002, Primitive, Active


726051002|Myotonia congenita (disorder)|
  • en Congenital myotonia
  • en Myotonia congenita
  • en Myotonia congenita (disorder)

726051002 |Myotonia congenita (disorder)|

<<< 66091009 |Congenital disease (disorder)| +
    193237003 |Myotonic disorder (disorder)| :
        { 363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
Active

3447741013 - Congenital myotonia (en) View

3447741013
en
Synonym (core metadata concept)
Congenital myotonia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

3447740014 - Myotonia congenita (en) View

3447740014
en
Synonym (core metadata concept)
Myotonia congenita
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3447739012 - Myotonia congenita (disorder) (en) View

3447739012
en
Fully specified name (core metadata concept)
Myotonia congenita (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

66091009 View

66091009
Congenital disease (disorder)
Congenital disease
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

193237003 View

193237003
Myotonic disorder (disorder)
Myotonic disorder
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

20305008 View

20305008
Congenital myotonia, autosomal recessive form (disorder)
Becker myotonia congenita
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

29145002 View

29145002
Schwartz-jampel syndrome (disorder)
Burton syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

57938005 View

57938005
Congenital myotonia, autosomal dominant form (disorder)
Thomsen's disease
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (412c304d-1bee-5615-b375-dad69f606167) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G71.1
TRUE
ALWAYS G71.1 | POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE
447561005 |Snomed ct source code to target map code correlation not specified (foundation metadata concept)|
447637006 |Map source concept is properly classified (foundation metadata concept)|
esc