Loading...
dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 784351000

Production
add
784351000
The component that hold information about this concept.
Antecubital pterygium syndrome (disorder)
Antecubital pterygium 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

Antecubital pterygium syndrome (disorder)

SCTID: 784351000, Primitive, Active


784351000|Antecubital pterygium syndrome (disorder)|
  • en Antecubital pterygium syndrome
  • en Antecubital pterygium syndrome (disorder)

784351000 |Antecubital pterygium syndrome (disorder)|

<<< 363070008 |Developmental hereditary disorder (disorder)| +
    66510004 |Congenital anomaly of upper limb (disorder)| +
    128133004 |Disorder of elbow (disorder)| +
    41443008 |Multiple malformation syndrome with limb defect as major feature (disorder)| +
    11164009 |Autosomal dominant hereditary disorder (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 76640006 |Congenital webbing (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 90837009 |Antecubital region structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
Active

3763739013 - Antecubital pterygium syndrome (en) View

3763739013
en
Synonym (core metadata concept)
Antecubital pterygium syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3763740010 - Antecubital pterygium syndrome (disorder) (en) View

3763740010
en
Fully specified name (core metadata concept)
Antecubital pterygium syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (13069767024) - 784351000 -> 363070008 (116680003) View

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

Relationship (11373076029) - 784351000 -> 11164009 (116680003) View

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

Relationship (11373077022) - 784351000 -> 308490002 (370135005) View

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

Relationship (11373078028) - 784351000 -> 255399007 (246454002) View

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

Relationship (11373079020) - 784351000 -> 76640006 (116676008) View

116676008 |Associated morphology (attribute)|
76640006 |Congenital webbing (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11373080023) - 784351000 -> 66510004 (116680003) View

116680003 |Is a (attribute)|
66510004 |Congenital anomaly of upper limb (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11373081022) - 784351000 -> 128133004 (116680003) View

116680003 |Is a (attribute)|
128133004 |Disorder of elbow (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11373082026) - 784351000 -> 41443008 (116680003) View

116680003 |Is a (attribute)|
41443008 |Multiple malformation syndrome with limb defect as major feature (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11373083020) - 784351000 -> 90837009 (363698007) View

363698007 |Finding site (attribute)|
90837009 |Antecubital region structure (body structure)|
1
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

128133004 View

128133004
Disorder of elbow (disorder)
Disease of elbow
900000000000073002 |Sufficiently defined by necessary conditions 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

41443008 View

41443008
Multiple malformation syndrome with limb defect as major feature (disorder)
Multiple malformation syndrome with limb defect as major feature
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

66510004 View

66510004
Congenital anomaly of upper limb (disorder)
Congenital anomaly of upper limb
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (fc442bc5-0f3c-54ab-a654-b186b913b33f) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q87.2
TRUE
ALWAYS Q87.2 | 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)|
esc