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204036008: Lissencephaly (disorder)

SNOMED CT Concept\Clinical finding\...

\Central nervous system finding\Finding of brain\Disorder of brain\Congenital anomaly of brain\Lissencephaly
\Central nervous system finding\Disorder of the central nervous system\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Lissencephaly
\Central nervous system finding\Disorder of the central nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\Lissencephaly
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Congenital anomaly of brain\Lissencephaly

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

\Finding of brain\Disorder of brain\Congenital anomaly of brain\Lissencephaly

\Disorder of head\Congenital anomaly of head\Congenital anomaly of brain\Lissencephaly
\Disorder of head\Disorder of brain\Congenital anomaly of brain\Lissencephaly

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

312882013 Lissencephaly en Synonym Active Entire term case insensitive SNOMED CT core module

312883015 Agyria en Synonym Active Entire term case insensitive SNOMED CT core module

312884014 Lissencephaly pachygyria en Synonym Active Entire term case insensitive SNOMED CT core module

312885010 Lissencephaly syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

589208018 Lissencephaly (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Lissencephaly	Is a	Congenital anomaly of head	false	Inferred relationship	Existential restriction modifier
Lissencephaly	Is a	Disorder of brain	false	Inferred relationship	Existential restriction modifier
Lissencephaly	Is a	Disorder of neuronal migration and differentiation	true	Inferred relationship	Existential restriction modifier
Lissencephaly	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier	1
Lissencephaly	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Lissencephaly	Finding site	Structure of central nervous system	false	Inferred relationship	Existential restriction modifier	1
Lissencephaly	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Lissencephaly	Is a	Congenital anomaly of brain	true	Inferred relationship	Existential restriction modifier
Lissencephaly	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Lissencephaly	Finding site	Brain structure	true	Inferred relationship	Existential restriction modifier	1
Lissencephaly	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Lissencephaly	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Lissencephaly	Finding site	Structure of nervous system	false	Inferred relationship	Existential restriction modifier	2
Lissencephaly	Is a	Disorder of brain	false	Inferred relationship	Existential restriction modifier
Lissencephaly	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	3
Lissencephaly	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	3
Lissencephaly	Finding site	Structure of central nervous system	false	Inferred relationship	Existential restriction modifier	3
Lissencephaly	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Lissencephaly	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
Lissencephaly	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Type 1 lissencephaly	Is a	True	Lissencephaly	Inferred relationship	Existential restriction modifier
Type 2 lissencephaly	Is a	True	Lissencephaly	Inferred relationship	Existential restriction modifier
Lissencephaly co-occurrent with congenital cerebellar hypoplasia	Is a	True	Lissencephaly	Inferred relationship	Existential restriction modifier
Craniotelencephalic dysplasia	Is a	True	Lissencephaly	Inferred relationship	Existential restriction modifier
X-linked lissencephaly with agenesis of corpus callosum and genital anomaly syndrome	Is a	True	Lissencephaly	Inferred relationship	Existential restriction modifier
Lissencephaly type 3 familial fetal akinesia sequence syndrome	Is a	False	Lissencephaly	Inferred relationship	Existential restriction modifier
Lissencephaly type 3 metacarpal bone dysplasia syndrome	Is a	True	Lissencephaly	Inferred relationship	Existential restriction modifier
Lissencephaly due to tubulin alpha 1A mutation	Is a	True	Lissencephaly	Inferred relationship	Existential restriction modifier
Microlissencephaly micromelia syndrome	Is a	True	Lissencephaly	Inferred relationship	Existential restriction modifier
Type 3 lissencephaly	Is a	True	Lissencephaly	Inferred relationship	Existential restriction modifier
Microlissencephaly	Is a	True	Lissencephaly	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
312882013	Lissencephaly	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
312883015	Agyria	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
312884014	Lissencephaly pachygyria	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
312885010	Lissencephaly syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
589208018	Lissencephaly (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module