51626007: Werner syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

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

\Premature aging 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 aging 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 aging 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 aging syndrome\Werner syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging 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 aging 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 aging syndrome\Werner syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary cancer-predisposing syndrome\Werner syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Premature aging 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 aging syndrome\Werner syndrome
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Premature aging syndrome\Werner syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging 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 aging syndrome\Werner syndrome
\Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with senile-like appearance\Werner syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\Werner syndrome
\Disease\Congenital disease\Inborn error of metabolism\Premature aging syndrome\Werner syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging 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 malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with senile-like appearance\Werner syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\Werner syndrome
\Disease\Developmental disorder\Disorder of stature\Werner syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

85980017 Werner syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

85981018 Progeria of the adult en Synonym Active Entire term case insensitive SNOMED CT core module

789546011 Werner syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

1231007018 Pangeria en Synonym Active Entire term case insensitive SNOMED CT core module

1231008011 Adult progeria en Synonym Active Entire term case insensitive SNOMED CT core module

1783826013 Adult premature ageing syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

1784214017 Adult premature aging syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Werner syndrome	Is a	Progeria	false	Inferred relationship	Existential restriction modifier
Werner syndrome	Is a	Multiple malformation syndrome with senile-like appearance	true	Inferred relationship	Existential restriction modifier
Werner syndrome	Is a	Disorder of stature	true	Inferred relationship	Existential restriction modifier
Werner syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Werner syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Werner syndrome	Is a	Congenital anomaly of skin	true	Inferred relationship	Existential restriction modifier
Werner syndrome	Is a	Premature aging syndrome	true	Inferred relationship	Existential restriction modifier
Werner syndrome	Associated morphology	Congenital malformation	false	Inferred relationship	Existential restriction modifier
Werner syndrome	Is a	Hereditary cancer-predisposing syndrome	true	Inferred relationship	Existential restriction modifier
Werner syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Werner syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	1
Werner syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
Werner syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Werner syndrome	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	1
Werner syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Werner syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier
Werner syndrome	Interprets	Height / growth measure	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
85980017	Werner syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
85981018	Progeria of the adult	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
789546011	Werner syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
1231007018	Pangeria	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1231008011	Adult progeria	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1783826013	Adult premature ageing syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1784214017	Adult premature aging syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module