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Terminology chevron_right Concepts chevron_right 236466005

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236466005
The component that hold information about this concept.
Congenital fanconi syndrome (disorder)
De toni-fanconi 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

Congenital fanconi syndrome (disorder)

SCTID: 236466005, Primitive, Active


236466005|Congenital fanconi syndrome (disorder)|
  • en Congenital fanconi syndrome
  • en Congenital fanconi syndrome (disorder)
  • en De toni-fanconi syndrome
  • en Primary fanconi syndrome

236466005 |Congenital fanconi syndrome (disorder)|

<<< 363039000 |Congenital connective tissue disorder (disorder)| +
    62332007 |Infantile nephropathic cystinosis (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 409774005 |Inflammatory morphology (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 50235001 |Structure of interstitial tissue of kidney (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 409774005 |Inflammatory morphology (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 58471003 |Renal tubule structure (body structure)| }
Active

354465019 - Congenital Fanconi syndrome (en) View

354465019
en
Synonym (core metadata concept)
Congenital Fanconi syndrome
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

625063019 - Congenital Fanconi syndrome (disorder) (en) View

625063019
en
Fully specified name (core metadata concept)
Congenital Fanconi syndrome (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

354463014 - De Toni-Fanconi syndrome (en) View

354463014
en
Synonym (core metadata concept)
De Toni-Fanconi syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

354464015 - Primary Fanconi syndrome (en) View

354464015
en
Synonym (core metadata concept)
Primary Fanconi syndrome
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

Relationship (522609022) - 236466005 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (12250049025) - 236466005 -> 363039000 (116680003) View

116680003 |Is a (attribute)|
363039000 |Congenital connective tissue disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12250050025) - 236466005 -> 255399007 (246454002) View

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

Relationship (522608025) - 236466005 -> 23583003 (116676008) View

116676008 |Associated morphology (attribute)|
23583003 |Inflammation (morphologic abnormality)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (3351062028) - 236466005 -> 23583003 (116676008) View

116676008 |Associated morphology (attribute)|
23583003 |Inflammation (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (5992165028) - 236466005 -> 29704000 (363698007) View

363698007 |Finding site (attribute)|
29704000 |Structure of parenchyma of kidney (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (12065338026) - 236466005 -> 409774005 (116676008) View

116676008 |Associated morphology (attribute)|
409774005 |Inflammatory morphology (morphologic abnormality)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12065339023) - 236466005 -> 58471003 (363698007) View

363698007 |Finding site (attribute)|
58471003 |Renal tubule structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12065340020) - 236466005 -> 409774005 (116676008) View

116676008 |Associated morphology (attribute)|
409774005 |Inflammatory morphology (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (522607024) - 236466005 -> 50235001 (363698007) View

363698007 |Finding site (attribute)|
50235001 |Structure of interstitial tissue of kidney (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (3459461026) - 236466005 -> 50235001 (363698007) View

363698007 |Finding site (attribute)|
50235001 |Structure of interstitial tissue of kidney (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (51528028) - 236466005 -> 62332007 (116680003) View

116680003 |Is a (attribute)|
62332007 |Infantile nephropathic cystinosis (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

363039000 View

363039000
Congenital connective tissue disorder (disorder)
Congenital connective tissue disorder
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

62332007 View

62332007
Infantile nephropathic cystinosis (disorder)
Nephropathic cystinosis
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (8f6ef4fb-9a67-5d7f-80c4-b3546c1ef0b1) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E72.0
TRUE
ALWAYS E72.0
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