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Terminology chevron_right Concepts chevron_right 765202001

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765202001
The component that hold information about this concept.
Familial multiple benign meningioma (disorder)
Familial multiple benign meningioma
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

Familial multiple benign meningioma (disorder)

SCTID: 765202001, Primitive, Active


765202001|Familial multiple benign meningioma (disorder)|
  • en Familial multiple benign meningioma
  • en Familial multiple benign meningioma (disorder)

765202001 |Familial multiple benign meningioma (disorder)|

<<< 11164009 |Autosomal dominant hereditary disorder (disorder)| +
    363235000 |Hereditary disorder of nervous system (disorder)| +
    724171006 |Benign meningioma (disorder)| +
    55352002 |Familial neoplastic disease (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 1157019008 |Benign meningioma (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 1231004 |Meninges structure (body structure)| }
Active

3657440013 - Familial multiple benign meningioma (en) View

3657440013
en
Synonym (core metadata concept)
Familial multiple benign meningioma
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3657439011 - Familial multiple benign meningioma (disorder) (en) View

3657439011
en
Fully specified name (core metadata concept)
Familial multiple benign meningioma (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (9238589022) - 765202001 -> 19453003 (116676008) View

116676008 |Associated morphology (attribute)|
19453003 |Meningioma, benign, no icd-o subtype (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (13822311024) - 765202001 -> 1157019008 (116676008) View

116676008 |Associated morphology (attribute)|
1157019008 |Benign meningioma (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9238586026) - 765202001 -> 11164009 (116680003) View

116680003 |Is a (attribute)|
11164009 |Autosomal dominant hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9238587024) - 765202001 -> 363235000 (116680003) View

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

Relationship (9238588025) - 765202001 -> 724171006 (116680003) View

116680003 |Is a (attribute)|
724171006 |Benign meningioma (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9238590029) - 765202001 -> 55352002 (116680003) View

116680003 |Is a (attribute)|
55352002 |Familial neoplastic disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9238591025) - 765202001 -> 1231004 (363698007) View

363698007 |Finding site (attribute)|
1231004 |Meninges structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

724171006 View

724171006
Benign meningioma (disorder)
Benign meningioma
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

11164009 View

11164009
Autosomal dominant hereditary disorder (disorder)
Ad - autosomal dominant
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

55352002 View

55352002
Familial neoplastic disease (disorder)
Familial neoplastic disease
900000000000073002 |Sufficiently defined by necessary conditions 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 (91b3691f-c6f9-5db8-9387-86a902b9f7df) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Z84.8
TRUE
ALWAYS Z84.8
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)|

ExtendedMap object (ccec9ea0-d0f2-5363-a9f0-529b9fc5681d) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D32.9
TRUE
ALWAYS D32.9 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | POSSIBLE REQUIREMENT FOR MORPHOLOGY 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