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Terminology chevron_right Concepts chevron_right 765197008

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765197008
The component that hold information about this concept.
Symptomatic form of muscular dystrophy of duchenne and becker in female carrier (disorder)
Symptomatic form of muscular dystrophy of duchenne and becker in female carrier
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

Symptomatic form of muscular dystrophy of duchenne and becker in female carrier (disorder)

SCTID: 765197008, Primitive, Active


765197008|Symptomatic form of muscular dystrophy of duchenne and becker in female carrier (disorder)|
  • en Symptomatic form of muscular dystrophy of duchenne and becker in female carrier
  • en Symptomatic form of muscular dystrophy of duchenne and becker in female carrier (disorder)

765197008 |Symptomatic form of muscular dystrophy of duchenne and becker in female carrier (disorder)|

<<< 240050008 |Manifesting female carrier of x-linked muscular dystrophy (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
Active

3657413013 - Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier (en) View

3657413013
en
Synonym (core metadata concept)
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3657415018 - Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier (disorder) (en) View

3657415018
en
Fully specified name (core metadata concept)
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

Relationship (11572551024) - 765197008 -> 255314001 (263502005) View

263502005 |Clinical course (attribute)|
255314001 |Progressive (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9238342021) - 765197008 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (9238343027) - 765197008 -> 21390004 (116676008) View

116676008 |Associated morphology (attribute)|
21390004 |Developmental anomaly (morphologic abnormality)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (9238344022) - 765197008 -> 127954009 (363698007) View

363698007 |Finding site (attribute)|
127954009 |Skeletal muscle structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (10533103029) - 765197008 -> 308490002 (370135005) View

370135005 |Pathological process (attribute)|
308490002 |Pathological developmental process (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9238338023) - 765197008 -> 4720007 (116676008) View

116676008 |Associated morphology (attribute)|
4720007 |Dystrophy (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9238339026) - 765197008 -> 127954009 (363698007) View

363698007 |Finding site (attribute)|
127954009 |Skeletal muscle structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9238340029) - 765197008 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9238341025) - 765197008 -> 240050008 (116680003) View

116680003 |Is a (attribute)|
240050008 |Manifesting female carrier of x-linked muscular dystrophy (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

240050008 View

240050008
Manifesting female carrier of x-linked muscular dystrophy (disorder)
Manifesting female carrier of x-linked muscular dystrophy
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (9ba60739-c7e1-55fb-9d24-ccd543d8636c) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G71.0
TRUE
ALWAYS G71.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
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