253149002: Type 2 lissencephaly (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Central nervous system finding\Disorder of the central nervous system (disorder)\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Lissencephaly\Type 2 lissencephaly
\Central nervous system finding\Disorder of the central nervous system (disorder)\Congenital anomaly of central nervous system\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly

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

\Finding of brain\Disorder of brain (disorder)\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly

\Disorder of head (disorder)\Congenital anomaly of head\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Disorder of head (disorder)\Disorder of brain (disorder)\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly

\Disease\Disorder of body system\Disorder of nervous system (disorder)\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Lissencephaly\Type 2 lissencephaly
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Lissencephaly\Type 2 lissencephaly
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Congenital anomaly of central nervous system\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Disease\Disorder of head (disorder)\Congenital anomaly of head\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Lissencephaly\Type 2 lissencephaly
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of head\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Lissencephaly\Type 2 lissencephaly
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of head\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly

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

Descriptions:

Id Description Lang Type Status Case? Module

377038012 Type 2 lissencephaly en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

643873011 Type 2 lissencephaly (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

1716521000052117 lissencefali typ 2 sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Type 2 lissencephaly	Is a	Lissencephaly	true	Inferred relationship	Some
Type 2 lissencephaly	Finding site	Brain structure	false	Inferred relationship	Some	1
Type 2 lissencephaly	Occurrence	Congenital	false	Inferred relationship	Some
Type 2 lissencephaly	Finding site	Structure of central nervous system (body structure)	false	Inferred relationship	Some	1
Type 2 lissencephaly	Associated morphology	kongenital anomali	false	Inferred relationship	Some	1
Type 2 lissencephaly	Associated morphology	kongenital anomali	false	Inferred relationship	Some	1
Type 2 lissencephaly	Finding site	Brain structure	true	Inferred relationship	Some	1
Type 2 lissencephaly	Occurrence	Congenital	false	Inferred relationship	Some	2
Type 2 lissencephaly	Associated morphology	utvecklingsabnormitet	false	Inferred relationship	Some	2
Type 2 lissencephaly	Finding site	Structure of nervous system (body structure)	false	Inferred relationship	Some	2
Type 2 lissencephaly	Occurrence	Congenital	false	Inferred relationship	Some	3
Type 2 lissencephaly	Associated morphology	utvecklingsabnormitet	false	Inferred relationship	Some	3
Type 2 lissencephaly	Finding site	Structure of central nervous system (body structure)	false	Inferred relationship	Some	3
Type 2 lissencephaly	Occurrence	Congenital	true	Inferred relationship	Some	1
Type 2 lissencephaly	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Type 2 lissencephaly	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Walker-Warburg congenital muscular dystrophy	Is a	True	Type 2 lissencephaly	Inferred relationship	Some
Cobblestone lissencephaly without muscular or ocular involvement (disorder)	Is a	True	Type 2 lissencephaly	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
377038012	Type 2 lissencephaly	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
643873011	Type 2 lissencephaly (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1716521000052117	lissencefali typ 2	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)