1259473000: Dementia due to fragile X syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Central nervous system finding\Finding of brain\Disorder of brain\Organic mental disorder\Dementia\Dementia associated with another disease\Dementia due to genetic disease\Dementia due to fragile X syndrome
\Central nervous system finding\Finding of brain\Disorder of brain\Organic mental disorder\Dementia\Dementia associated with another disease\Dementia due to chromosomal anomaly\Dementia due to fragile X syndrome
\Central nervous system finding\Disorder of the central nervous system\Central nervous system complication\Dementia associated with another disease\Dementia due to genetic disease\Dementia due to fragile X syndrome
\Central nervous system finding\Disorder of the central nervous system\Central nervous system complication\Dementia associated with another disease\Dementia due to chromosomal anomaly\Dementia due to fragile X syndrome
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Organic mental disorder\Dementia\Dementia associated with another disease\Dementia due to genetic disease\Dementia due to fragile X syndrome
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Organic mental disorder\Dementia\Dementia associated with another disease\Dementia due to chromosomal anomaly\Dementia due to fragile X syndrome

\Finding of head and neck region\Head finding\...

\Finding of brain\Disorder of brain\Organic mental disorder\Dementia\Dementia associated with another disease\...

\Dementia due to genetic disease\Dementia due to fragile X syndrome

\Dementia due to chromosomal anomaly\Dementia due to fragile X syndrome

\Disorder of head\Disorder of brain\Organic mental disorder\Dementia\Dementia associated with another disease\...

\Dementia due to genetic disease\Dementia due to fragile X syndrome

\Dementia due to chromosomal anomaly\Dementia due to fragile X syndrome

\Functional finding\Cognitive function finding\Impaired cognition\Dementia\Dementia associated with another disease\...

\Dementia due to genetic disease\Dementia due to fragile X syndrome

\Dementia due to chromosomal anomaly\Dementia due to fragile X syndrome

\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Central nervous system complication\Dementia associated with another disease\Dementia due to genetic disease\Dementia due to fragile X syndrome
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Central nervous system complication\Dementia associated with another disease\Dementia due to chromosomal anomaly\Dementia due to fragile X syndrome
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Organic mental disorder\Dementia\Dementia associated with another disease\Dementia due to genetic disease\Dementia due to fragile X syndrome
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Organic mental disorder\Dementia\Dementia associated with another disease\Dementia due to chromosomal anomaly\Dementia due to fragile X syndrome
\Disease\Disorder of head\Disorder of brain\Organic mental disorder\Dementia\Dementia associated with another disease\Dementia due to genetic disease\Dementia due to fragile X syndrome
\Disease\Disorder of head\Disorder of brain\Organic mental disorder\Dementia\Dementia associated with another disease\Dementia due to chromosomal anomaly\Dementia due to fragile X syndrome
\Disease\Mental disorder\Organic mental disorder\Dementia\Dementia associated with another disease\Dementia due to genetic disease\Dementia due to fragile X syndrome
\Disease\Mental disorder\Organic mental disorder\Dementia\Dementia associated with another disease\Dementia due to chromosomal anomaly\Dementia due to fragile X syndrome

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2023. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

5157110012 Dementia due to fragile X syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

5159446019 Dementia due to fragile X syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Dementia due to fragile X syndrome	Is a	Dementia due to chromosomal anomaly	true	Inferred relationship	Existential restriction modifier
Dementia due to fragile X syndrome	Due to	Fragile X syndrome	true	Inferred relationship	Existential restriction modifier	3
Dementia due to fragile X syndrome	Finding site	Brain structure	true	Inferred relationship	Existential restriction modifier	2
Dementia due to fragile X syndrome	Interprets	Cognitive functions	true	Inferred relationship	Existential restriction modifier	1
Dementia due to fragile X syndrome	Has interpretation	Impaired	true	Inferred relationship	Existential restriction modifier	1
Dementia due to fragile X syndrome	Is a	Dementia due to genetic disease	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
5157110012	Dementia due to fragile X syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
5159446019	Dementia due to fragile X syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module