238875009: Wrinkly skin syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\...

\Premature ageing syndrome\Wrinkly skin syndrome

\Congenital anomaly of skin\Wrinkly skin syndrome

\General finding of soft tissue\Skin finding\Disorder of skin\Premature ageing syndrome\Wrinkly skin syndrome
\General finding of soft tissue\Skin finding\Disorder of skin\Congenital anomaly of skin\Wrinkly skin syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Wrinkly skin syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Wrinkly skin syndrome

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Premature ageing syndrome\Wrinkly skin syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Wrinkly skin syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Wrinkly skin syndrome
\Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Wrinkly skin syndrome
\Integumentary system finding\Skin finding\Disorder of skin\Premature ageing syndrome\Wrinkly skin syndrome
\Integumentary system finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Wrinkly skin syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Premature ageing syndrome\Wrinkly skin syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Premature ageing syndrome\Wrinkly skin syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Wrinkly skin syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Wrinkly skin syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Premature ageing syndrome\Wrinkly skin syndrome
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Premature ageing syndrome\Wrinkly skin syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Wrinkly skin syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Wrinkly skin syndrome
\Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Wrinkly skin syndrome
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Premature ageing syndrome\Wrinkly skin syndrome
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Wrinkly skin syndrome
\Disease\Congenital disease\Inborn error of metabolism\Premature ageing syndrome\Wrinkly skin syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Wrinkly skin syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Wrinkly skin syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Wrinkly skin syndrome
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Wrinkly skin syndrome

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

Descriptions:

Id Description Lang Type Status Case? Module

358006018 WSS - Wrinkly skin syndrome en Synonym Active Case sensitive SNOMED CT core

358007010 Wrinkly skin syndrome en Synonym Active Case insensitive SNOMED CT core

627814018 Wrinkly skin syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Wrinkly skin syndrome	Associated morphology	Wrinkle	false	Inferred relationship	Some	2
Wrinkly skin syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Wrinkly skin syndrome	Finding site	Skin structure	true	Inferred relationship	Some	1
Wrinkly skin syndrome	Associated morphology	Wrinkle	true	Inferred relationship	Some	1
Wrinkly skin syndrome	Is a	Congenital anomaly of skin	true	Inferred relationship	Some
Wrinkly skin syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Some
Wrinkly skin syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Wrinkly skin syndrome	Is a	Premature ageing syndrome	true	Inferred relationship	Some
Wrinkly skin syndrome	Occurrence	Congenital	true	Inferred relationship	Some	1
Wrinkly skin syndrome	Finding site	Skin structure	false	Inferred relationship	Some	2
Wrinkly skin syndrome	Is a	Progeria syndrome	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

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
358006018	WSS - Wrinkly skin syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
358007010	Wrinkly skin syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
627814018	Wrinkly skin syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core