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Terminology chevron_right Concepts chevron_right 718122005

Production
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718122005
The component that hold information about this concept.
Piebaldism (disorder)
Piebaldism
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

Piebaldism (disorder)

SCTID: 718122005, Primitive, Active


718122005|Piebaldism (disorder)|
  • en Piebaldism
  • en Piebaldism (disorder)

718122005 |Piebaldism (disorder)|

<<< 1953005 |Congenital deficiency of pigment of skin (disorder)| +
    11164009 |Autosomal dominant hereditary disorder (disorder)| +
    363185004 |Hereditary disorder of the integument (disorder)| +
    724839001 |Genetic disorder of skin pigmentation (disorder)| +
    363070008 |Developmental hereditary disorder (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 89031001 |Hypopigmentation (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

3311231014 - Piebaldism (en) View

3311231014
en
Synonym (core metadata concept)
Piebaldism
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3311230010 - Piebaldism (disorder) (en) View

3311230010
en
Fully specified name (core metadata concept)
Piebaldism (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (6594904022) - 718122005 -> 363185004 (116680003) View

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

Relationship (13069667028) - 718122005 -> 363070008 (116680003) View

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

Relationship (6594905023) - 718122005 -> 83386001 (116676008) View

116676008 |Associated morphology (attribute)|
83386001 |Congenital hypopigmentation (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (10517355029) - 718122005 -> 308490002 (370135005) View

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

Relationship (11183298023) - 718122005 -> 89031001 (116676008) View

116676008 |Associated morphology (attribute)|
89031001 |Hypopigmentation (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6920329022) - 718122005 -> 724839001 (116680003) View

116680003 |Is a (attribute)|
724839001 |Genetic disorder of skin pigmentation (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6594902021) - 718122005 -> 1953005 (116680003) View

116680003 |Is a (attribute)|
1953005 |Congenital deficiency of pigment of skin (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6594903027) - 718122005 -> 11164009 (116680003) View

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

Relationship (6594906024) - 718122005 -> 255399007 (246454002) View

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

Relationship (6594907026) - 718122005 -> 39937001 (363698007) View

363698007 |Finding site (attribute)|
39937001 |Skin 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

724839001 View

724839001
Genetic disorder of skin pigmentation (disorder)
Genetic disorder of skin pigmentation
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

1953005 View

1953005
Congenital deficiency of pigment of skin (disorder)
Congenital deficiency of pigment of skin
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

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

ExtendedMap object (b88ae64b-7e3a-5777-aac8-a386ad408f80) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E70.3
TRUE
ALWAYS E70.3
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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