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Terminology chevron_right Concepts chevron_right 782823001

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782823001
The component that hold information about this concept.
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome (disorder)
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition 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

Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome (disorder)

SCTID: 782823001, Primitive, Active


782823001|Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome (disorder)|
  • en Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome
  • en Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome (disorder)

782823001 |Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome (disorder)|

<<< 1197432002 |Telangiectasia of skin (disorder)| +
    363005004 |Cardiovascular system hereditary disorder (disorder)| +
    11164009 |Autosomal dominant hereditary disorder (disorder)| +
    363185004 |Hereditary disorder of the integument (disorder)| +
    111941005 |Familial disease (disorder)| +
    699346009 |Hereditary cancer-predisposing syndrome (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 112641009 |Telangiectasis (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 360599008 |Microscopic skin vascular structure (body structure)| }
Active

3756078013 - Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome (en) View

3756078013
en
Synonym (core metadata concept)
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3756077015 - Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome (disorder) (en) View

3756077015
en
Fully specified name (core metadata concept)
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (11227966028) - 782823001 -> 247479008 (116680003) View

116680003 |Is a (attribute)|
247479008 |Telangiectasia disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (15029803025) - 782823001 -> 1197432002 (116680003) View

116680003 |Is a (attribute)|
1197432002 |Telangiectasia of skin (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11227962026) - 782823001 -> 11164009 (116680003) View

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

Relationship (11227963020) - 782823001 -> 112641009 (116676008) View

116676008 |Associated morphology (attribute)|
112641009 |Telangiectasis (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11227964025) - 782823001 -> 360599008 (363698007) View

363698007 |Finding site (attribute)|
360599008 |Microscopic skin vascular structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11227965029) - 782823001 -> 363185004 (116680003) View

116680003 |Is a (attribute)|
363185004 |Hereditary disorder of the integument (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11227967021) - 782823001 -> 111941005 (116680003) View

116680003 |Is a (attribute)|
111941005 |Familial disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11227968027) - 782823001 -> 699346009 (116680003) View

116680003 |Is a (attribute)|
699346009 |Hereditary cancer-predisposing syndrome (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11227969024) - 782823001 -> 363005004 (116680003) View

116680003 |Is a (attribute)|
363005004 |Cardiovascular system hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

1197432002 View

1197432002
Telangiectasia of skin (disorder)
Telangiectasia of skin
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

699346009 View

699346009
Hereditary cancer-predisposing syndrome (disorder)
Hereditary neoplastic 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

111941005 View

111941005
Familial disease (disorder)
Familial disease
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

363005004 View

363005004
Cardiovascular system hereditary disorder (disorder)
Cardiovascular system hereditary disorder
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

363185004 View

363185004
Hereditary disorder of the integument (disorder)
Hereditary disorder of the integument
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True
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