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Terminology chevron_right Concepts chevron_right 55602000

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55602000
The component that hold information about this concept.
Nezelof's syndrome (disorder)
Nezelof syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Nezelof's syndrome (disorder)

SCTID: 55602000, Primitive, Active


55602000|Nezelof's syndrome (disorder)|
  • en Congenital thymic dysplasia syndrome
  • en Nezelof syndrome
  • en Nezelof's syndrome (disorder)
  • en Nezelof's syndrome

55602000 |Nezelof's syndrome (disorder)|

<<< 31323000 |Severe combined immunodeficiency disease (disorder)| :
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 91689009 |Body system structure (body structure)| }
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
Active

92426011 - Congenital thymic dysplasia syndrome (en) View

92426011
en
Synonym (core metadata concept)
Congenital thymic dysplasia syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

2840435013 - Nezelof syndrome (en) View

2840435013
en
Synonym (core metadata concept)
Nezelof syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

793991019 - Nezelof's syndrome (disorder) (en) View

793991019
en
Fully specified name (core metadata concept)
Nezelof's syndrome (disorder)
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

92425010 - Nezelof's syndrome (en) View

92425010
en
Synonym (core metadata concept)
Nezelof's syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

Relationship (811835022) - 55602000 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (2734428024) - 55602000 -> 91689009 (363698007) View

363698007 |Finding site (attribute)|
91689009 |Body system structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11171444024) - 55602000 -> 769247005 (370135005) View

370135005 |Pathological process (attribute)|
769247005 |Abnormal immune process (qualifier value)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (2734429027) - 55602000 -> 106182000 (363705008) View

363705008 |Has definitional manifestation (attribute)|
106182000 |Immune system finding (finding)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (811836023) - 55602000 -> 24484000 (246112005) View

246112005 |Severity (attribute)|
24484000 |Severe (severity modifier) (qualifier value)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (811837025) - 55602000 -> 116003000 (363698007) View

363698007 |Finding site (attribute)|
116003000 |Structure of immune system (body structure)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (238514022) - 55602000 -> 31323000 (116680003) View

116680003 |Is a (attribute)|
31323000 |Severe combined immunodeficiency disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

31323000 View

31323000
Severe combined immunodeficiency disease (disorder)
Scid
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (9da1efff-9a58-51c7-ae04-9aef3b9be9ee) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D81.4
TRUE
ALWAYS D81.4
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)|
esc