238836000: Kindler's syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Hereditary sclerosing poikiloderma\Kindler's syndrome

\General finding of soft tissue\Skin finding\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Hereditary sclerosing poikiloderma\Kindler's syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Hereditary sclerosing poikiloderma\Kindler's syndrome

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Hereditary sclerosing poikiloderma\Kindler's syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Hereditary sclerosing poikiloderma\Kindler's syndrome
\Integumentary system finding\Skin finding\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Hereditary sclerosing poikiloderma\Kindler's syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary sclerosing poikiloderma\Kindler's syndrome
\Disease\Degenerative disorder\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Hereditary sclerosing poikiloderma\Kindler's syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary sclerosing poikiloderma\Kindler's syndrome
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Hereditary sclerosing poikiloderma\Kindler's syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Hereditary sclerosing poikiloderma\Kindler's syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Hereditary sclerosing poikiloderma\Kindler's syndrome

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2840887018 Kindler syndrome en Synonym Active Case sensitive SNOMED CT core

357953015 Kindler's syndrome en Synonym Active Case sensitive SNOMED CT core

627771014 Kindler's syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Kindler's syndrome	Is a	Degenerative disorder	false	Inferred relationship	Some
Kindler's syndrome	Is a	Atrophic condition of skin	false	Inferred relationship	Some
Kindler's syndrome	Finding site	Skin structure	true	Inferred relationship	Some	1
Kindler's syndrome	Associated morphology	Poikiloderma	true	Inferred relationship	Some	1
Kindler's syndrome	Associated morphology	Poikiloderma	false	Inferred relationship	Some	1
Kindler's syndrome	Finding site	Skin structure	false	Inferred relationship	Some	1
Kindler's syndrome	Is a	Hereditary sclerosing poikiloderma	true	Inferred relationship	Some
Kindler's syndrome	Is a	Skin lesion	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set