230786001: Congenital dysphasia (disorder)

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

\Head finding (finding)\Finding of brain\Disorder of brain\Congenital dysphasia
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Congenital dysphasia

\Central nervous system finding\Finding of brain\Disorder of brain\Congenital dysphasia
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Congenital dysphasia

\Speech finding\Disturbance in speech\Dysphasia\Congenital dysphasia

\Neurological finding\Aphasia, agnosia, dyslexia AND/OR apraxia\Dyslexia AND/OR speech dysfunction\Dysphasia\Congenital dysphasia

\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital dysphasia
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Congenital dysphasia
\Disease\Disorder of head (disorder)\Disorder of brain\Congenital dysphasia

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

345787014 Congenital dysphasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

618640013 Congenital dysphasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

345787014 Congenital dysphasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

345787014 Congenital dysphasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

618640013 Congenital dysphasia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

618640013 Congenital dysphasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

76791000077117 dysphasie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

76791000077117 dysphasie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital dysphasia	Is a	Disorder of brain	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital dysphasia	Is a	Congenital anomaly of head	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital dysphasia	Finding site	The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica.	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital dysphasia	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital dysphasia	Is a	Congenital disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital dysphasia	Is a	Dysphasia	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital dysphasia	Finding site	The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica.	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital dysphasia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital dysphasia	Interprets	Speech observable (observable entity)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Congenital expressive dysphasia	Is a	True	Congenital dysphasia	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital receptive dysphasia	Is a	True	Congenital dysphasia	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets