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Terminology chevron_right Concepts chevron_right 773394007

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773394007
The component that hold information about this concept.
Autosomal recessive frontotemporal pachygyria (disorder)
Autosomal recessive frontotemporal pachygyria
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

Autosomal recessive frontotemporal pachygyria (disorder)

SCTID: 773394007, Primitive, Active


773394007|Autosomal recessive frontotemporal pachygyria (disorder)|
  • en Autosomal recessive frontotemporal pachygyria
  • en Autosomal recessive frontotemporal pachygyria (disorder)

773394007 |Autosomal recessive frontotemporal pachygyria (disorder)|

<<< 85995004 |Autosomal recessive hereditary disorder (disorder)| +
    23024003 |Macrogyria (disorder)| +
    363235000 |Hereditary disorder of nervous system (disorder)| +
    363070008 |Developmental hereditary disorder (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 442021009 |Enlargement (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 279165009 |Structure of cerebral gyrus (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
Active

3723363018 - Autosomal recessive frontotemporal pachygyria (en) View

3723363018
en
Synonym (core metadata concept)
Autosomal recessive frontotemporal pachygyria
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3723362011 - Autosomal recessive frontotemporal pachygyria (disorder) (en) View

3723362011
en
Fully specified name (core metadata concept)
Autosomal recessive frontotemporal pachygyria (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (13069974020) - 773394007 -> 363070008 (116680003) View

116680003 |Is a (attribute)|
363070008 |Developmental hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10599261025) - 773394007 -> 441880008 (116676008) View

116676008 |Associated morphology (attribute)|
441880008 |Congenital enlargement (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (11300998029) - 773394007 -> 442021009 (116676008) View

116676008 |Associated morphology (attribute)|
442021009 |Enlargement (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10599258026) - 773394007 -> 279165009 (363698007) View

363698007 |Finding site (attribute)|
279165009 |Structure of cerebral gyrus (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10599259023) - 773394007 -> 308490002 (370135005) View

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

Relationship (10599260029) - 773394007 -> 85995004 (116680003) View

116680003 |Is a (attribute)|
85995004 |Autosomal recessive hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10599262021) - 773394007 -> 363235000 (116680003) View

116680003 |Is a (attribute)|
363235000 |Hereditary disorder of nervous system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10599263027) - 773394007 -> 255399007 (246454002) View

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

Relationship (10599264022) - 773394007 -> 23024003 (116680003) View

116680003 |Is a (attribute)|
23024003 |Macrogyria (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

363070008 View

363070008
Developmental hereditary disorder (disorder)
Developmental hereditary disorder
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

23024003 View

23024003
Macrogyria (disorder)
Macrogyria
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

85995004 View

85995004
Autosomal recessive hereditary disorder (disorder)
Hereditary disorder trait, nos
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

363235000 View

363235000
Hereditary disorder of nervous system (disorder)
Hereditary disorder of nervous system
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (b5ccd12b-1614-5bb1-8764-fafa4dc141ed) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q04.3
TRUE
ALWAYS Q04.3 | 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