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773329005: CK syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Mental state, behavior and/or psychosocial function finding\Behavior finding\Intellectual disability\CK syndrome

\Functional finding\Cognitive function finding\Impaired cognition\Intellectual disability\CK syndrome
\Functional finding\Cognitive function finding\Finding of intellectual ability\Intellectual disability\CK syndrome
\Functional finding\Intelligence finding\Finding of intellectual ability\Intellectual disability\CK syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\CK syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\CK syndrome
\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\CK syndrome
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\CK syndrome
\Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid metabolism\CK syndrome
\Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\CK syndrome
\Disease\Congenital disease\Inborn error of metabolism\CK syndrome
\Disease\Developmental disorder\Neurodevelopmental disorder\Intellectual disability\CK syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\CK syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\CK syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3723193016 CK syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

3723194010 X-linked intellectual disability, microcephaly, cortical malformation, thin habitus syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

3723199017 CK syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
CK syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
CK syndrome	Is a	Intellectual disability	true	Inferred relationship	Existential restriction modifier
CK syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
CK syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
CK syndrome	Is a	X-linked hereditary disease	false	Inferred relationship	Existential restriction modifier
CK syndrome	Is a	Multiple system malformation syndrome	true	Inferred relationship	Existential restriction modifier
CK syndrome	Is a	Inborn error of metabolism	true	Inferred relationship	Existential restriction modifier
CK syndrome	Is a	Disorder of lipid metabolism	true	Inferred relationship	Existential restriction modifier
CK syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier
CK syndrome	Is a	X-linked recessive hereditary disease	true	Inferred relationship	Existential restriction modifier
CK syndrome	Interprets	Intellectual ability	true	Inferred relationship	Existential restriction modifier	2
CK syndrome	Has interpretation	Impaired	true	Inferred relationship	Existential restriction modifier	2
CK syndrome	Interprets	Adaptation behavior	true	Inferred relationship	Existential restriction modifier	3
CK syndrome	Has interpretation	Impaired	true	Inferred relationship	Existential restriction modifier	3

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
3723193016	CK syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3723194010	X-linked intellectual disability, microcephaly, cortical malformation, thin habitus syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3723199017	CK syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module