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277922001: Aprosencephaly (disorder)

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

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

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Aprosencephaly	Is a	Abnormality of neurogenesis	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Aprosencephaly	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Aprosencephaly	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Aprosencephaly	Is a	Congenital anomaly of brain	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Aprosencephaly	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Aprosencephaly	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Aprosencephaly	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Aprosencephaly	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Aprosencephaly	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Aprosencephaly	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Aprosencephaly	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Aprosencephaly	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Aprosencephaly	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Aprosencephaly	Finding site	Structure of diencephalon	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Aprosencephaly	Is a	Aprosencephaly/atelencephaly spectrum	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Aprosencephaly	Finding site	Structure of telencephalon (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Aprosencephaly	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Aprosencephaly	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

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

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
414666013	Aprosencephaly	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
671015014	Aprosencephaly (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
414666013	Aprosencephaly	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
414666013	Aprosencephaly	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
671015014	Aprosencephaly (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
671015014	Aprosencephaly (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
671015014	Aprosencephaly (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5128921000241112	aprosencéphalie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5128921000241112	aprosencéphalie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module