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Terminology chevron_right Concepts chevron_right 724002003

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724002003
The component that hold information about this concept.
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder)
Rambaud gallian 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

Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder)

SCTID: 724002003, Primitive, Active


724002003|Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder)|
  • en Rambaud gallian syndrome
  • en Rambaud gallian touchard syndrome
  • en Retinal ischaemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome
  • en Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome
  • en Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder)

724002003 |Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder)|

<<< 17944005 |Cerebral calcification (disorder)| +
    26468004 |Retinal ischemia (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    280871000 |Vascular degeneration (disorder)| +
    363005004 |Cardiovascular system hereditary disorder (disorder)| +
    363343008 |Hereditary disorder of the visual system (disorder)| +
    106018006 |Hereditary degenerative disease of central nervous system (disorder)|
        { 363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 19010006 |Hyaline degeneration (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 27915009 |Structure of small blood vessel (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 18115005 |Pathologic calcification, calcified structure (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 83678007 |Cerebral structure (body structure)| }
Active

3428521014 - Rambaud Gallian syndrome (en) View

3428521014
en
Synonym (core metadata concept)
Rambaud Gallian syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

3428522019 - Rambaud Gallian Touchard syndrome (en) View

3428522019
en
Synonym (core metadata concept)
Rambaud Gallian Touchard syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

3428524018 - Retinal ischaemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (en) View

3428524018
en
Synonym (core metadata concept)
Retinal ischaemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

3428523012 - Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (en) View

3428523012
en
Synonym (core metadata concept)
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

3428520010 - Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder) (en) View

3428520010
en
Fully specified name (core metadata concept)
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (6870453025) - 724002003 -> 363235000 (116680003) View

116680003 |Is a (attribute)|
363235000 |Hereditary disorder of nervous system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (12091759024) - 724002003 -> 106018006 (116680003) View

116680003 |Is a (attribute)|
106018006 |Hereditary degenerative disease of central nervous system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6870455021) - 724002003 -> 5665001 (363698007) View

363698007 |Finding site (attribute)|
5665001 |Retinal structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6870448024) - 724002003 -> 17944005 (116680003) View

116680003 |Is a (attribute)|
17944005 |Cerebral calcification (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6870449027) - 724002003 -> 26468004 (116680003) View

116680003 |Is a (attribute)|
26468004 |Retinal ischemia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6870450027) - 724002003 -> 85995004 (116680003) View

116680003 |Is a (attribute)|
85995004 |Autosomal recessive hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6870451028) - 724002003 -> 280871000 (116680003) View

116680003 |Is a (attribute)|
280871000 |Vascular degeneration (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6870452024) - 724002003 -> 363005004 (116680003) View

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

Relationship (6870454020) - 724002003 -> 363343008 (116680003) View

116680003 |Is a (attribute)|
363343008 |Hereditary disorder of the visual system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6870458023) - 724002003 -> 19010006 (116676008) View

116676008 |Associated morphology (attribute)|
19010006 |Hyaline degeneration (morphologic abnormality)|
4
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6870459026) - 724002003 -> 27915009 (363698007) View

363698007 |Finding site (attribute)|
27915009 |Structure of small blood vessel (body structure)|
4
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6874141027) - 724002003 -> 18115005 (116676008) View

116676008 |Associated morphology (attribute)|
18115005 |Pathologic calcification, calcified structure (morphologic abnormality)|
5
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6874142023) - 724002003 -> 83678007 (363698007) View

363698007 |Finding site (attribute)|
83678007 |Cerebral structure (body structure)|
5
900000000000011006 |Inferred relationship (core metadata concept)|
True

106018006 View

106018006
Hereditary degenerative disease of central nervous system (disorder)
Hereditary degenerative disease of central nervous system
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

17944005 View

17944005
Cerebral calcification (disorder)
Cerebral calcification
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

26468004 View

26468004
Retinal ischemia (disorder)
Retinal pallor
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

85995004 View

85995004
Autosomal recessive hereditary disorder (disorder)
Hereditary disorder trait, nos
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

280871000 View

280871000
Vascular degeneration (disorder)
Vascular degeneration
900000000000073002 |Sufficiently defined by necessary conditions 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

363343008 View

363343008
Hereditary disorder of the visual system (disorder)
Hereditary disorder of the visual system
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True
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