253149002: Type 2 lissencephaly (disorder)

SNOMED CT Concept\Clinical finding\...

\Central nervous system finding\Finding of brain\Disorder of brain\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Central nervous system finding\Disorder of the central nervous system\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\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 of brain\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly

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

\Finding of brain\Disorder of brain\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly

\Disorder of head\Congenital anomaly of head\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Disorder of head\Disorder of brain\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly

\Disease\Disorder of body system\Disorder of nervous system\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\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 of the central 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 of the central 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 of the central nervous system\Disorder of brain\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Disease\Disorder of head\Disorder of brain\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Disease\Congenital disease\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\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\Lissencephaly\Type 2 lissencephaly
\Disease\Congenital disease\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. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

377038012 Type 2 lissencephaly en Synonym Active Entire term case sensitive SNOMED CT core module

643873011 Type 2 lissencephaly (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
Type 2 lissencephaly	Is a	Lissencephaly	true	Inferred relationship	Existential restriction modifier
Type 2 lissencephaly	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier	1
Type 2 lissencephaly	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Type 2 lissencephaly	Finding site	Structure of central nervous system	false	Inferred relationship	Existential restriction modifier	1
Type 2 lissencephaly	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Type 2 lissencephaly	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Type 2 lissencephaly	Finding site	Brain structure	true	Inferred relationship	Existential restriction modifier	1
Type 2 lissencephaly	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Type 2 lissencephaly	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Type 2 lissencephaly	Finding site	Structure of nervous system	false	Inferred relationship	Existential restriction modifier	2
Type 2 lissencephaly	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	3
Type 2 lissencephaly	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	3
Type 2 lissencephaly	Finding site	Structure of central nervous system	false	Inferred relationship	Existential restriction modifier	3
Type 2 lissencephaly	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Type 2 lissencephaly	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Type 2 lissencephaly	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Walker-Warburg congenital muscular dystrophy	Is a	True	Type 2 lissencephaly	Inferred relationship	Existential restriction modifier
Cobblestone lissencephaly without muscular or ocular involvement	Is a	True	Type 2 lissencephaly	Inferred relationship	Existential restriction modifier

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