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Terminology chevron_right Concepts chevron_right 65071000119106

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65071000119106
The component that hold information about this concept.
Family history of fragile x syndrome (situation)
Family history of fragile x syndrome
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 fragile x syndrome (situation)

SCTID: 65071000119106, Defined, Active


65071000119106|Family history of fragile x syndrome (situation)|
  • vi Tiền sử gia đình mắc hội chứng x dễ gãy
  • en Family history of fragile x syndrome
  • en Family history of fragile x syndrome (situation)

65071000119106 |Family history of fragile x syndrome (situation)|

=== 160425006 |Family history: chromosomal anomaly (situation)| +
    64731000119106 |Family history of multiple congenital anomalies (situation)| +
    763598005 |Family history of intellectual disability (situation)| +
    429962007 |Family history of hereditary disease (situation)| :
        { 246090004 |Associated finding (attribute)| = 613003 |Fragile x 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

472781000003113 - tiền sử gia đình mắc hội chứng X dễ gãy (vi) View

472781000003113
vi
Synonym (core metadata concept)
tiền sử gia đình mắc hội chứng X dễ gãy
900000000000448009 |Entire term case insensitive (core metadata concept)|
None
True

3078055019 - Family history of fragile X syndrome (en) View

3078055019
en
Synonym (core metadata concept)
Family history of fragile X syndrome
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3078051011 - Family history of fragile X syndrome (situation) (en) View

3078051011
en
Fully specified name (core metadata concept)
Family history of fragile X syndrome (situation)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

Relationship (6226871025) - 65071000119106 -> 444148008 (408732007) View

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

Relationship (15279615029) - 65071000119106 -> 303071001 (408732007) View

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

Relationship (12088359028) - 65071000119106 -> 763598005 (116680003) View

116680003 |Is a (attribute)|
763598005 |Family history of intellectual disability (situation)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12088360022) - 65071000119106 -> 429962007 (116680003) View

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

Relationship (6968946027) - 65071000119106 -> 64731000119106 (116680003) View

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

Relationship (6226869025) - 65071000119106 -> 160425006 (116680003) View

116680003 |Is a (attribute)|
160425006 |Family history: chromosomal anomaly (situation)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6226870029) - 65071000119106 -> 613003 (246090004) View

246090004 |Associated finding (attribute)|
613003 |Fragile x syndrome (disorder)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6226872021) - 65071000119106 -> 410511007 (408731000) View

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

Relationship (6226873027) - 65071000119106 -> 410515003 (408729009) View

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

763598005 View

763598005
Family history of intellectual disability (situation)
Tiền sử gia đình bị thiểu năng trí tuệ
900000000000073002 |Sufficiently defined by necessary conditions definition status (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

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

160425006 View

160425006
Family history: chromosomal anomaly (situation)
Fh: chromosomal anomaly
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (979a1e9b-604f-5f04-acb1-f6c55a99515c) 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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