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277922001: Aprosencephaly (disorder)

SNOMED CT Concept\Clinical finding\...

\Central nervous system finding\Finding of brain\Disorder of brain\Congenital anomaly of brain\Congenital anomaly of cerebrum\Aprosencephaly/atelencephaly spectrum\Aprosencephaly
\Central nervous system finding\Disorder of the central nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\Congenital anomaly of cerebrum\Aprosencephaly/atelencephaly spectrum\Aprosencephaly
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Congenital anomaly of brain\Congenital anomaly of cerebrum\Aprosencephaly/atelencephaly spectrum\Aprosencephaly

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

\Finding of brain\Disorder of brain\Congenital anomaly of brain\Congenital anomaly of cerebrum\Aprosencephaly/atelencephaly spectrum\Aprosencephaly

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

414666013 Aprosencephaly en Synonym Active Entire term case insensitive SNOMED CT core module

671015014 Aprosencephaly (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
Aprosencephaly	Is a	Abnormality of neurogenesis	false	Inferred relationship	Existential restriction modifier
Aprosencephaly	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Aprosencephaly	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier	1
Aprosencephaly	Is a	Congenital anomaly of brain	false	Inferred relationship	Existential restriction modifier
Aprosencephaly	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Aprosencephaly	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Aprosencephaly	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier	1
Aprosencephaly	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Aprosencephaly	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Aprosencephaly	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier	2
Aprosencephaly	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Aprosencephaly	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
Aprosencephaly	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Aprosencephaly	Finding site	Structure of diencephalon	true	Inferred relationship	Existential restriction modifier	1
Aprosencephaly	Is a	Aprosencephaly/atelencephaly spectrum	true	Inferred relationship	Existential restriction modifier
Aprosencephaly	Finding site	Structure of telencephalon	true	Inferred relationship	Existential restriction modifier	2
Aprosencephaly	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	2
Aprosencephaly	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
XK aprosencephaly syndrome	Is a	True	Aprosencephaly	Inferred relationship	Existential restriction modifier
Aprosencephaly cerebellar dysgenesis	Is a	True	Aprosencephaly	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
414666013	Aprosencephaly	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
671015014	Aprosencephaly (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module