715633008: Atypical Werner syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Atypical Werner syndrome

\General finding of soft tissue\Skin finding\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Atypical Werner syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Atypical Werner syndrome

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Premature aging syndrome\Laminopathy with premature aging\Atypical Werner syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Atypical Werner syndrome
\Integumentary system finding\Skin finding\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Atypical Werner syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Premature aging syndrome\Laminopathy with premature aging\Atypical Werner syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Premature aging syndrome\Laminopathy with premature aging\Atypical Werner syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Premature aging syndrome\Laminopathy with premature aging\Atypical Werner syndrome
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Premature aging syndrome\Laminopathy with premature aging\Atypical Werner syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Atypical Werner syndrome
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Premature aging syndrome\Laminopathy with premature aging\Atypical Werner syndrome
\Disease\Congenital disease\Inborn error of metabolism\Premature aging syndrome\Laminopathy with premature aging\Atypical Werner syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Atypical Werner syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3303243012 Atypical Werner syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

3303244018 Atypical Werner syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module

3303245017 Atypical progeroid syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Atypical Werner syndrome	Is a	Premature aging syndrome	false	Inferred relationship	Existential restriction modifier
Atypical Werner syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Atypical Werner syndrome	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	2
Atypical Werner syndrome	Is a	Laminopathy with premature aging	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets