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Terminology chevron_right Concepts chevron_right 783013001

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783013001
The component that hold information about this concept.
Parana hard skin syndrome (disorder)
Parana hard 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

Parana hard skin syndrome (disorder)

SCTID: 783013001, Primitive, Active


783013001|Parana hard skin syndrome (disorder)|
  • en Hard skin syndrome parana type
  • en Parana hard skin syndrome
  • en Parana hard skin syndrome (disorder)

783013001 |Parana hard skin syndrome (disorder)|

<<< 17417006 |Thickening of skin (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    128236002 |Chronic disease of skin (disorder)| +
    363185004 |Hereditary disorder of the integument (disorder)| +
    363212003 |Hereditary disorder of musculoskeletal system (disorder)| +
    38850007 |Chronic arthropathy (disorder)| :
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 39352004 |Joint structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)| }
Active

3757145012 - Hard skin syndrome Parana type (en) View

3757145012
en
Synonym (core metadata concept)
Hard skin syndrome Parana type
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

3757144011 - Parana hard skin syndrome (en) View

3757144011
en
Synonym (core metadata concept)
Parana hard skin syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

3757143017 - Parana hard skin syndrome (disorder) (en) View

3757143017
en
Fully specified name (core metadata concept)
Parana hard skin syndrome (disorder)
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

Relationship (11271660028) - 783013001 -> 17417006 (116680003) View

116680003 |Is a (attribute)|
17417006 |Thickening of skin (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11271661029) - 783013001 -> 85995004 (116680003) View

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

Relationship (11271663026) - 783013001 -> 128236002 (116680003) View

116680003 |Is a (attribute)|
128236002 |Chronic disease of skin (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11271665022) - 783013001 -> 363185004 (116680003) View

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

Relationship (11271666023) - 783013001 -> 363212003 (116680003) View

116680003 |Is a (attribute)|
363212003 |Hereditary disorder of musculoskeletal system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11271668024) - 783013001 -> 38850007 (116680003) View

116680003 |Is a (attribute)|
38850007 |Chronic arthropathy (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11573742020) - 783013001 -> 39352004 (363698007) View

363698007 |Finding site (attribute)|
39352004 |Joint structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11573743026) - 783013001 -> 255314001 (263502005) View

263502005 |Clinical course (attribute)|
255314001 |Progressive (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11573744021) - 783013001 -> 39937001 (363698007) View

363698007 |Finding site (attribute)|
39937001 |Skin structure (body structure)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

17417006 View

17417006
Thickening of skin (disorder)
Thickening of skin
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

38850007 View

38850007
Chronic arthropathy (disorder)
Bệnh khớp mạn tính
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

128236002 View

128236002
Chronic disease of skin (disorder)
Chronic dermatosis
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

363212003 View

363212003
Hereditary disorder of musculoskeletal system (disorder)
Hereditary disorder of musculoskeletal system
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (3fe6449a-7cf6-5141-9e7a-8a787d502821) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
L91.8
TRUE
ALWAYS L91.8 | 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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