1237365009: Aprosencephaly/atelencephaly spectrum (disorder)

SNOMED CT Concept\Clinical finding\...

\Central nervous system finding\Finding of brain\Encephalopathy\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\Encephalopathy\Congenital anomaly of brain\Congenital anomaly of cerebrum\Aprosencephaly/atelencephaly spectrum

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

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

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

Status: current, Primitive. Date: 30-Sep 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

5098002015 Aprosencephaly/atelencephaly spectrum en Synonym Active Case insensitive SNOMED CT core

5098003013 Aprosencephaly/atelencephaly spectrum (disorder) en Fully specified name Active Case insensitive SNOMED CT core

5098004019 A group of rare central nervous system malformations with characteristics of varying degrees of absence or dysplasia of the derivatives of the prosencephalon (i.e. telencephalon and diencephalon), with an intact cranial vault. The spectrum comprises atelencephaly, the less severe form, in which only the telencephalon is affected, and aprosencephaly, where the diencephalon is also involved. The malformations may occur in an isolated form or in association with other anomalies. en Definition Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Aprosencephaly/atelencephaly spectrum	Is a	Abnormality of neurogenesis	true	Inferred relationship	Some
Aprosencephaly/atelencephaly spectrum	Is a	Disorder of embryonic structure	true	Inferred relationship	Some
Aprosencephaly/atelencephaly spectrum	Is a	Congenital anomaly of cerebrum	true	Inferred relationship	Some
Aprosencephaly/atelencephaly spectrum	Occurrence	Congenital	true	Inferred relationship	Some	1
Aprosencephaly/atelencephaly spectrum	Finding site	Prosencephalon structure	true	Inferred relationship	Some	1
Aprosencephaly/atelencephaly spectrum	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Some	1
Aprosencephaly/atelencephaly spectrum	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1

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

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
5098002015	Aprosencephaly/atelencephaly spectrum	en	Synonym	Active	Case insensitive	SNOMED CT core
5098003013	Aprosencephaly/atelencephaly spectrum (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
5098004019	A group of rare central nervous system malformations with characteristics of varying degrees of absence or dysplasia of the derivatives of the prosencephalon (i.e. telencephalon and diencephalon), with an intact cranial vault. The spectrum comprises atelencephaly, the less severe form, in which only the telencephalon is affected, and aprosencephaly, where the diencephalon is also involved. The malformations may occur in an isolated form or in association with other anomalies.	en	Definition	Active	Case sensitive	SNOMED CT core