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Terminology chevron_right Concepts chevron_right 64731000119106

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64731000119106
The component that hold information about this concept.
Family history of multiple congenital anomalies (situation)
Tiền sử gia đình đa dị tật bẩm sinh
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 multiple congenital anomalies (situation)

SCTID: 64731000119106, Defined, Active


64731000119106|Family history of multiple congenital anomalies (situation)|
  • vi Tiền sử gia đình đa dị tật bẩm sinh
  • en Family history of multiple congenital anomalies
  • en Family history of multiple congenital anomalies (situation)

64731000119106 |Family history of multiple congenital anomalies (situation)|

=== 597941000005106 |Family history of congenital malformation (situation)| :
        { 246090004 |Associated finding (attribute)| = 400038003 |Congenital malformation syndrome (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

444721000003119 - tiền sử gia đình đa dị tật bẩm sinh (vi) View

444721000003119
vi
Synonym (core metadata concept)
tiền sử gia đình đa dị tật bẩm sinh
900000000000448009 |Entire term case insensitive (core metadata concept)|
None
True

3467198016 - Family history of multiple congenital anomalies (en) View

3467198016
en
Synonym (core metadata concept)
Family history of multiple congenital anomalies
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3467197014 - Family history of multiple congenital anomalies (situation) (en) View

3467197014
en
Fully specified name (core metadata concept)
Family history of multiple congenital anomalies (situation)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (6968932027) - 64731000119106 -> 160417009 (116680003) View

116680003 |Is a (attribute)|
160417009 |Family history: congenital anomaly (situation)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (11290880029) - 64731000119106 -> 412749001 (116680003) View

116680003 |Is a (attribute)|
412749001 |Family history of development disorder (situation)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (16019711023) - 64731000119106 -> 597941000005106 (116680003) View

116680003 |Is a (attribute)|
597941000005106 |Family history of congenital malformation (situation)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6968936029) - 64731000119106 -> 444148008 (408732007) View

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

Relationship (15279532023) - 64731000119106 -> 303071001 (408732007) View

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

Relationship (6968933021) - 64731000119106 -> 400038003 (246090004) View

246090004 |Associated finding (attribute)|
400038003 |Congenital malformation syndrome (disorder)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6968934026) - 64731000119106 -> 410515003 (408729009) View

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

Relationship (6968935025) - 64731000119106 -> 410511007 (408731000) View

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

597941000005106 View

597941000005106
Family history of congenital malformation (situation)
Family history of congenital malformation
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

65031000119108 View

65031000119108
Family history of cowden syndrome (situation)
Tiền sử gia đình hội chứng cowden
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

64121000119107 View

64121000119107
Family history of achondroplasia (situation)
Tiền sử gia đình loạn sản sụn
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

64851000119105 View

64851000119105
Family history of prader-willi syndrome (situation)
Family history of prader-willi syndrome
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

65071000119106 View

65071000119106
Family history of fragile x syndrome (situation)
Family history of fragile x syndrome
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (9053e7e5-f468-583f-8af2-05a9d54bdd21) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Z82.7
TRUE
ALWAYS Z82.7
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