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Terminology chevron_right Concepts chevron_right 717766000

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717766000
The component that hold information about this concept.
Alport syndrome autosomal dominant (disorder)
Alport syndrome autosomal dominant
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

Alport syndrome autosomal dominant (disorder)

SCTID: 717766000, Primitive, Active


717766000|Alport syndrome autosomal dominant (disorder)|
  • en Alport syndrome autosomal dominant
  • en Alport syndrome autosomal dominant (disorder)

717766000 |Alport syndrome autosomal dominant (disorder)|

<<< 770414008 |Alport syndrome (disorder)| +
    11164009 |Autosomal dominant hereditary disorder (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 409777003 |Chronic inflammatory morphology (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 68288006 |Glomerulus structure (body structure)| }
        { 363714003 |Interprets (attribute)| = 47078008 |Hearing, function (observable entity)| }
        { 363698007 |Finding site (attribute)| = 91159003 |Structure of auditory system (body structure)| }
        { 42752001 |Due to (attribute)| = 32895009 |Hereditary disease (disorder)| }
Active

3310200014 - Alport syndrome autosomal dominant (en) View

3310200014
en
Synonym (core metadata concept)
Alport syndrome autosomal dominant
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

3306956019 - Alport syndrome autosomal dominant (disorder) (en) View

3306956019
en
Fully specified name (core metadata concept)
Alport syndrome autosomal dominant (disorder)
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

Relationship (16376453024) - 717766000 -> 32895009 (42752001) View

42752001 |Due to (attribute)|
32895009 |Hereditary disease (disorder)|
4
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6680118021) - 717766000 -> 84499006 (116676008) View

116676008 |Associated morphology (attribute)|
84499006 |Chronic inflammation (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (15816873022) - 717766000 -> 409777003 (116676008) View

116676008 |Associated morphology (attribute)|
409777003 |Chronic inflammatory morphology (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9618374027) - 717766000 -> 47078008 (363714003) View

363714003 |Interprets (attribute)|
47078008 |Hearing, function (observable entity)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9618376025) - 717766000 -> 91159003 (363698007) View

363698007 |Finding site (attribute)|
91159003 |Structure of auditory system (body structure)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6680117027) - 717766000 -> 399340005 (116680003) View

116680003 |Is a (attribute)|
399340005 |Hereditary nephritis (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (9618375026) - 717766000 -> 770414008 (116680003) View

116680003 |Is a (attribute)|
770414008 |Alport syndrome (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6680116020) - 717766000 -> 11164009 (116680003) View

116680003 |Is a (attribute)|
11164009 |Autosomal dominant hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6680119029) - 717766000 -> 68288006 (363698007) View

363698007 |Finding site (attribute)|
68288006 |Glomerulus structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

770414008 View

770414008
Alport syndrome (disorder)
Alport syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

11164009 View

11164009
Autosomal dominant hereditary disorder (disorder)
Ad - autosomal dominant
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (d95684ef-8d2e-548e-870f-e6cc43448c70) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q87.8
TRUE
ALWAYS Q87.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
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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