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Terminology chevron_right Concepts chevron_right 64391000119106

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64391000119106
The component that hold information about this concept.
Family history of hemoglobinopathy e (situation)
Family history of hemoglobinopathy e
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 hemoglobinopathy e (situation)

SCTID: 64391000119106, Defined, Active


64391000119106|Family history of hemoglobinopathy e (situation)|
  • vi Tiền sử gia đình mắc bệnh hemoglobin e
  • en Family history of haemoglobin e disease
  • en Family history of haemoglobinopathy e
  • en Family history of hemoglobin e disease
  • en Family history of hemoglobinopathy e
  • en Family history of hemoglobinopathy e (situation)

64391000119106 |Family history of hemoglobinopathy e (situation)|

=== 64501000119109 |Family history of hemoglobinopathy (situation)| +
    160417009 |Family history: congenital anomaly (situation)| +
    429962007 |Family history of hereditary disease (situation)| :
        { 246090004 |Associated finding (attribute)| = 25065001 |Hemoglobin e disease (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

441121000003115 - tiền sử gia đình mắc bệnh hemoglobin E (vi) View

441121000003115
vi
Synonym (core metadata concept)
tiền sử gia đình mắc bệnh hemoglobin E
900000000000448009 |Entire term case insensitive (core metadata concept)|
None
True

3438785011 - Family history of haemoglobin E disease (en) View

3438785011
en
Synonym (core metadata concept)
Family history of haemoglobin E disease
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

3438784010 - Family history of haemoglobinopathy E (en) View

3438784010
en
Synonym (core metadata concept)
Family history of haemoglobinopathy E
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

3438783016 - Family history of hemoglobin E disease (en) View

3438783016
en
Synonym (core metadata concept)
Family history of hemoglobin E disease
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

3438782014 - Family history of hemoglobinopathy E (en) View

3438782014
en
Synonym (core metadata concept)
Family history of hemoglobinopathy E
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

3438781019 - Family history of hemoglobinopathy E (situation) (en) View

3438781019
en
Fully specified name (core metadata concept)
Family history of hemoglobinopathy E (situation)
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

Relationship (6882674022) - 64391000119106 -> 444148008 (408732007) View

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

Relationship (15279531027) - 64391000119106 -> 303071001 (408732007) View

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

Relationship (6882669025) - 64391000119106 -> 429962007 (116680003) View

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

Relationship (6882670029) - 64391000119106 -> 64501000119109 (116680003) View

116680003 |Is a (attribute)|
64501000119109 |Family history of hemoglobinopathy (situation)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6882671025) - 64391000119106 -> 25065001 (246090004) View

246090004 |Associated finding (attribute)|
25065001 |Hemoglobin e disease (disorder)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6882672021) - 64391000119106 -> 410515003 (408729009) View

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

Relationship (6882673027) - 64391000119106 -> 410511007 (408731000) View

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

Relationship (7008693023) - 64391000119106 -> 160417009 (116680003) View

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

64501000119109 View

64501000119109
Family history of hemoglobinopathy (situation)
Family history of hemoglobinopathy
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

160417009 View

160417009
Family history: congenital anomaly (situation)
Fh: congenital anomaly
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (624a50b9-a867-5788-b012-93d6a1d8f0d2) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Z83.2
TRUE
ALWAYS Z83.2
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