51626007: Werner syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

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

\Premature ageing syndrome\Werner syndrome

\Congenital anomaly of skin\Werner syndrome

\Finding of general physiological development\Disorder of stature\Werner syndrome

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

\General finding of observation of patient\Body measurement finding\Height / growth finding\General finding of height\Disorder of stature\Werner syndrome

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

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Premature ageing syndrome\Werner syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary neoplastic syndrome\Werner syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Premature ageing syndrome\Werner syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Werner syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Werner syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Premature ageing syndrome\Werner syndrome
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Premature ageing syndrome\Werner syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Werner syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Werner syndrome
\Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Werner syndrome
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Premature ageing syndrome\Werner syndrome
\Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with senile-like appearance\Werner syndrome
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Werner syndrome
\Disease\Congenital disease\Inborn error of metabolism\Premature ageing syndrome\Werner syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Werner syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Werner syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Werner syndrome
\Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with senile-like appearance\Werner syndrome
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Werner syndrome
\Disease\Developmental disorder\Disorder of stature\Werner syndrome

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

Descriptions:

Id Description Lang Type Status Case? Module

1231007018 Pangeria en Synonym Active Case insensitive SNOMED CT core
1231008011 Adult progeria en Synonym Active Case insensitive SNOMED CT core
1783826013 Adult premature ageing syndrome en Synonym Active Case insensitive SNOMED CT core
1784214017 Adult premature aging syndrome en Synonym Active Case insensitive SNOMED CT core
789546011 Werner syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core
85980017 Werner syndrome en Synonym Active Case sensitive SNOMED CT core
85981018 Progeria of the adult en Synonym Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Werner syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Some	1
Werner syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Werner syndrome	Finding site	Skin structure	true	Inferred relationship	Some	1
Werner syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Werner syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Some
Werner syndrome	Interprets	Height / growth measure	true	Inferred relationship	Some	2
Werner syndrome	Is a	Congenital anomaly of skin	true	Inferred relationship	Some
Werner syndrome	Is a	Premature ageing syndrome	true	Inferred relationship	Some
Werner syndrome	Associated morphology	Congenital malformation	false	Inferred relationship	Some
Werner syndrome	Is a	Progeria syndrome	false	Inferred relationship	Some
Werner syndrome	Is a	Multiple malformation syndrome with senile-like appearance	true	Inferred relationship	Some
Werner syndrome	Is a	Disorder of stature	true	Inferred relationship	Some
Werner syndrome	Is a	Hereditary neoplastic syndrome	true	Inferred relationship	Some
Werner syndrome	Occurrence	Congenital	true	Inferred relationship	Some	1
Werner syndrome	Associated morphology	Developmental abnormality	false	Inferred relationship	Some	1
Werner syndrome	Finding site	Skin structure	false	Inferred relationship	Some	2
Werner syndrome	Occurrence	Congenital	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
1231007018	Pangeria	en	Synonym	Active	Case insensitive	SNOMED CT core
1231008011	Adult progeria	en	Synonym	Active	Case insensitive	SNOMED CT core
1783826013	Adult premature ageing syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
1784214017	Adult premature aging syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
789546011	Werner syndrome (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
85980017	Werner syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
85981018	Progeria of the adult	en	Synonym	Active	Case insensitive	SNOMED CT core