1237365009: Aprosencephaly/atelencephaly spectrum (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
\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
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Congenital anomaly of brain\Congenital anomaly of cerebrum\Aprosencephaly/atelencephaly spectrum

\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

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

\Disease\Disorder of embryonic structure\Aprosencephaly/atelencephaly spectrum
\Disease\Disorder of body system\Disorder of nervous system\Congenital anomaly of nervous system\Abnormality of neurogenesis\Aprosencephaly/atelencephaly spectrum
\Disease\Disorder of body system\Disorder of nervous system\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\Congenital anomaly of cerebrum\Aprosencephaly/atelencephaly spectrum
\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\Congenital anomaly of cerebrum\Aprosencephaly/atelencephaly spectrum
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Congenital anomaly of brain\Congenital anomaly of cerebrum\Aprosencephaly/atelencephaly spectrum
\Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of brain\Congenital anomaly of cerebrum\Aprosencephaly/atelencephaly spectrum
\Disease\Disorder of head\Disorder of brain\Congenital anomaly of brain\Congenital anomaly of cerebrum\Aprosencephaly/atelencephaly spectrum
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of nervous system\Abnormality of neurogenesis\Aprosencephaly/atelencephaly spectrum
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\Congenital anomaly of cerebrum\Aprosencephaly/atelencephaly spectrum
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of brain\Congenital anomaly of cerebrum\Aprosencephaly/atelencephaly spectrum
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of nervous system\Abnormality of neurogenesis\Aprosencephaly/atelencephaly spectrum
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\Congenital anomaly of cerebrum\Aprosencephaly/atelencephaly spectrum
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of head\Congenital anomaly of brain\Congenital anomaly of cerebrum\Aprosencephaly/atelencephaly spectrum

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

5098002015 Aprosencephaly/atelencephaly spectrum en Synonym Active Entire term case insensitive SNOMED CT core module

5098003013 Aprosencephaly/atelencephaly spectrum (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/atelencephaly spectrum	Is a	Abnormality of neurogenesis	true	Inferred relationship	Existential restriction modifier
Aprosencephaly/atelencephaly spectrum	Is a	Disorder of embryonic structure	true	Inferred relationship	Existential restriction modifier
Aprosencephaly/atelencephaly spectrum	Is a	Congenital anomaly of cerebrum	true	Inferred relationship	Existential restriction modifier
Aprosencephaly/atelencephaly spectrum	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Aprosencephaly/atelencephaly spectrum	Finding site	Prosencephalon structure	true	Inferred relationship	Existential restriction modifier	1
Aprosencephaly/atelencephaly spectrum	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
Aprosencephaly/atelencephaly spectrum	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Atelencephaly	Is a	True	Aprosencephaly/atelencephaly spectrum	Inferred relationship	Existential restriction modifier
Aprosencephaly	Is a	True	Aprosencephaly/atelencephaly spectrum	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
5098002015	Aprosencephaly/atelencephaly spectrum	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
5098003013	Aprosencephaly/atelencephaly spectrum (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module