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Terminology chevron_right Concepts chevron_right 64121000119107

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64121000119107
The component that hold information about this concept.
Family history of achondroplasia (situation)
Tiền sử gia đình loạn sản sụn
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 achondroplasia (situation)

SCTID: 64121000119107, Defined, Active


64121000119107|Family history of achondroplasia (situation)|
  • vi Tiền sử gia đình loạn sản sụn
  • en Family history of achondroplasia
  • en Family history of achondroplasia (situation)

64121000119107 |Family history of achondroplasia (situation)|

=== 160424005 |Family history: congenital orthopedic anomaly (context-dependent category)| +
    69731000119107 |Family history of short stature (situation)| +
    64731000119106 |Family history of multiple congenital anomalies (situation)| +
    429962007 |Family history of hereditary disease (situation)| :
        { 246090004 |Associated finding (attribute)| = 86268005 |Achondroplasia (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

457401000003112 - tiền sử gia đình loạn sản sụn (vi) View

457401000003112
vi
Synonym (core metadata concept)
tiền sử gia đình loạn sản sụn
900000000000448009 |Entire term case insensitive (core metadata concept)|
None
True

3038238017 - Family history of achondroplasia (en) View

3038238017
en
Synonym (core metadata concept)
Family history of achondroplasia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3038226014 - Family history of achondroplasia (situation) (en) View

3038226014
en
Fully specified name (core metadata concept)
Family history of achondroplasia (situation)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (6026143024) - 64121000119107 -> 444148008 (408732007) View

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

Relationship (15279599028) - 64121000119107 -> 303071001 (408732007) View

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

Relationship (12877491026) - 64121000119107 -> 429962007 (116680003) View

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

Relationship (11226684022) - 64121000119107 -> 64731000119106 (116680003) View

116680003 |Is a (attribute)|
64731000119106 |Family history of multiple congenital anomalies (situation)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6026141021) - 64121000119107 -> 65001000119101 (116680003) View

116680003 |Is a (attribute)|
65001000119101 |Family history of connective tissue disorder (situation)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6026139020) - 64121000119107 -> 160424005 (116680003) View

116680003 |Is a (attribute)|
160424005 |Family history: congenital orthopedic anomaly (context-dependent category)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6026142025) - 64121000119107 -> 86268005 (246090004) View

246090004 |Associated finding (attribute)|
86268005 |Achondroplasia (disorder)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6026144029) - 64121000119107 -> 410511007 (408731000) View

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

Relationship (6026145028) - 64121000119107 -> 410515003 (408729009) View

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

Relationship (6048825021) - 64121000119107 -> 69731000119107 (116680003) View

116680003 |Is a (attribute)|
69731000119107 |Family history of short stature (situation)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

64731000119106 View

64731000119106
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)|
True

69731000119107 View

69731000119107
Family history of short stature (situation)
Family history of short stature
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

429962007 View

429962007
Family history of hereditary disease (situation)
Family history of genetic disease
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

160424005 View

160424005
Family history: congenital orthopedic anomaly (context-dependent category)
Fh: cong. orthopedic anomaly
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (25a3b5bc-10f7-51ac-a8cc-bce975dead40) 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)|
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