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Terminology chevron_right Concepts chevron_right 98011000119108

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  • Language with ID “973a3efa-bd3c-5dd0-8a19-913e456d011e” doesn’t exist. Perhaps it was deleted?
98011000119108
The component that hold information about this concept.
Family history of butyrylcholinesterase deficiency (situation)
Family history of pseudocholinesterase deficiency
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Family history of butyrylcholinesterase deficiency (situation)

SCTID: 98011000119108, Defined, Active


98011000119108|Family history of butyrylcholinesterase deficiency (situation)|
  • vi Tiền sử gia đình thiếu enzyme đặc hiệu cholinesterase
  • en Family history of butyrylcholinesterase deficiency
  • en Family history of butyrylcholinesterase deficiency (situation)
  • en Family history of pseudocholinesterase deficiency

98011000119108 |Family history of butyrylcholinesterase deficiency (situation)|

=== 160305008 |Family history of metabolic disorder (situation)| :
        { 246090004 |Associated finding (attribute)| = 360619001 |Deficiency of butyrylcholinesterase (disorder)|,
          408729009 |Finding context (attribute)| = 410515003 |Known present (qualifier value)|,
          408732007 |Subject relationship context (attribute)| = 303071001 |Person in the family (person)|,
          408731000 |Temporal context (attribute)| = 410511007 |Current or past (actual) (qualifier value)| }
Active

449311000003114 - tiền sử gia đình thiếu enzyme đặc hiệu cholinesterase (vi) View

449311000003114
vi
Synonym (core metadata concept)
tiền sử gia đình thiếu enzyme đặc hiệu cholinesterase
900000000000448009 |Entire term case insensitive (core metadata concept)|
None
True

3788091010 - Family history of butyrylcholinesterase deficiency (en) View

3788091010
en
Synonym (core metadata concept)
Family history of butyrylcholinesterase deficiency
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3788092015 - Family history of butyrylcholinesterase deficiency (situation) (en) View

3788092015
en
Fully specified name (core metadata concept)
Family history of butyrylcholinesterase deficiency (situation)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3042724017 - Family history of pseudocholinesterase deficiency (situation) (en) View

3042724017
en
Fully specified name (core metadata concept)
Family history of pseudocholinesterase deficiency (situation)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
False

3042477014 - Family history of pseudocholinesterase deficiency (en) View

3042477014
en
Synonym (core metadata concept)
Family history of pseudocholinesterase deficiency
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

Relationship (6046192020) - 98011000119108 -> 444148008 (408732007) View

408732007 |Subject relationship context (attribute)|
444148008 |Person in family of subject (person)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (15279628020) - 98011000119108 -> 303071001 (408732007) View

408732007 |Subject relationship context (attribute)|
303071001 |Person in the family (person)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6046188029) - 98011000119108 -> 266907002 (116680003) View

116680003 |Is a (attribute)|
266907002 |Family history: musculoskeletal disease (context-dependent category)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6046189021) - 98011000119108 -> 429962007 (116680003) View

116680003 |Is a (attribute)|
429962007 |Family history of hereditary disease (situation)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6046190028) - 98011000119108 -> 297239000 (116680003) View

116680003 |Is a (attribute)|
297239000 |Family history of neurological disorder (situation)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6046191029) - 98011000119108 -> 191397007 (246090004) View

246090004 |Associated finding (attribute)|
191397007 |Pseudocholinesterase deficiency (disorder)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (12097885020) - 98011000119108 -> 160305008 (116680003) View

116680003 |Is a (attribute)|
160305008 |Family history of metabolic disorder (situation)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12097886021) - 98011000119108 -> 360619001 (246090004) View

246090004 |Associated finding (attribute)|
360619001 |Deficiency of butyrylcholinesterase (disorder)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6046193026) - 98011000119108 -> 410511007 (408731000) View

408731000 |Temporal context (attribute)|
410511007 |Current or past (actual) (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6046194021) - 98011000119108 -> 410515003 (408729009) View

408729009 |Finding context (attribute)|
410515003 |Known present (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

160305008 View

160305008
Family history of metabolic disorder (situation)
Fh: metabolic disorder
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (a6c7b10a-5e9a-556b-827b-120a0eb33ee1) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Z83.4
TRUE
ALWAYS Z83.4
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)|
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