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Terminology chevron_right Concepts chevron_right 238875009

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238875009
The component that hold information about this concept.
Wrinkly skin syndrome (disorder)
Wrinkly skin 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

Wrinkly skin syndrome (disorder)

SCTID: 238875009, Primitive, Active


238875009|Wrinkly skin syndrome (disorder)|
  • en Wrinkly skin syndrome
  • en Wrinkly skin syndrome (disorder)
  • en Wss - wrinkly skin syndrome

238875009 |Wrinkly skin syndrome (disorder)|

<<< 85995004 |Autosomal recessive hereditary disorder (disorder)| +
    199879009 |Congenital anomaly of skin (disorder)| +
    363070008 |Developmental hereditary disorder (disorder)| +
    399959003 |Premature aging syndrome (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 27367001 |Wrinkled structure (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
Active

358007010 - Wrinkly skin syndrome (en) View

358007010
en
Synonym (core metadata concept)
Wrinkly skin syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

627814018 - Wrinkly skin syndrome (disorder) (en) View

627814018
en
Fully specified name (core metadata concept)
Wrinkly skin syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

358006018 - WSS - Wrinkly skin syndrome (en) View

358006018
en
Synonym (core metadata concept)
WSS - Wrinkly skin syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

Relationship (530061023) - 238875009 -> 39937001 (363698007) View

363698007 |Finding site (attribute)|
39937001 |Skin structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (12128441020) - 238875009 -> 27367001 (116676008) View

116676008 |Associated morphology (attribute)|
27367001 |Wrinkled structure (morphologic abnormality)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (13275106025) - 238875009 -> 85995004 (116680003) View

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

Relationship (13275107023) - 238875009 -> 39937001 (363698007) View

363698007 |Finding site (attribute)|
39937001 |Skin structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (13275108029) - 238875009 -> 27367001 (116676008) View

116676008 |Associated morphology (attribute)|
27367001 |Wrinkled structure (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (13275119026) - 238875009 -> 199879009 (116680003) View

116680003 |Is a (attribute)|
199879009 |Congenital anomaly of skin (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (13275120021) - 238875009 -> 363070008 (116680003) View

116680003 |Is a (attribute)|
363070008 |Developmental hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (13275121020) - 238875009 -> 308490002 (370135005) View

370135005 |Pathological process (attribute)|
308490002 |Pathological developmental process (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (530060024) - 238875009 -> 255399007 (246454002) View

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

Relationship (54914029) - 238875009 -> 190590004 (116680003) View

116680003 |Is a (attribute)|
190590004 |Progeria (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2220025023) - 238875009 -> 399959003 (116680003) View

116680003 |Is a (attribute)|
399959003 |Premature aging syndrome (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

363070008 View

363070008
Developmental hereditary disorder (disorder)
Developmental hereditary disorder
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

399959003 View

399959003
Premature aging syndrome (disorder)
Premature aging syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

199879009 View

199879009
Congenital anomaly of skin (disorder)
Genodermatosis, nos
900000000000073002 |Sufficiently defined by necessary conditions 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
esc