278849000: Cerebral atrophy (disorder)

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

\Head finding (finding)\Finding of brain\Disorder of brain\Degenerative brain disorder\Cerebral degeneration (disorder)\Cerebral atrophy (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Degenerative brain disorder\Cerebral degeneration (disorder)\Cerebral atrophy (disorder)

\Central nervous system finding\Finding of brain\Disorder of brain\Degenerative brain disorder\Cerebral degeneration (disorder)\Cerebral atrophy (disorder)
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Degenerative brain disorder\Cerebral degeneration (disorder)\Cerebral atrophy (disorder)
\Central nervous system finding\Disorder of the central nervous system (disorder)\Degenerative disease of the central nervous system\Degenerative brain disorder\Cerebral degeneration (disorder)\Cerebral atrophy (disorder)

\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Degenerative brain disorder\Cerebral degeneration (disorder)\Cerebral atrophy (disorder)
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Degenerative brain disorder\Cerebral degeneration (disorder)\Cerebral atrophy (disorder)
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Degenerative disease of the central nervous system\Degenerative brain disorder\Cerebral degeneration (disorder)\Cerebral atrophy (disorder)
\Disease\Disorder of head (disorder)\Disorder of brain\Degenerative brain disorder\Cerebral degeneration (disorder)\Cerebral atrophy (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Cerebral atrophy (disorder)	Is a	Disorder of brain	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Cerebral atrophy (disorder)	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)
Cerebral atrophy (disorder)	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Cerebral atrophy (disorder)	Is a	Degenerative disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Cerebral atrophy (disorder)	Associated morphology	Atrophy	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Cerebral atrophy (disorder)	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
Cerebral atrophy (disorder)	Is a	Cerebral degeneration (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Arteriopathic granular atrophy of cerebral cortex	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Circumscribed atrophy of brain	Is a	False	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder)	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Pick's disease	Is a	False	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Atrophy of corpus callosum	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Acquired cerebral atrophy (disorder)	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Keratosis follicularis, dwarfism, cerebral atrophy syndrome (disorder)	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder)	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Progressive focal cortical atrophy	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome (disorder)	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal recessive cerebral atrophy (disorder)	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
A rare genetic neurometabolic disorder with characteristics of severe progressive microcephaly, severe to profound global development delay, intellectual disability, seizures (typically tonic and/or myoclonic and frequently intractable), hyperekplexia and axial hypotonia with appendicular spasticity, as well as hyperreflexia, dyskinetic quadriplegia and abnormal brain morphology (cerebral atrophy with variable additional features including ventriculomegaly, pons and/or cerebellar hypoplasia, simplified gyral pattern and delayed myelination). Cortical blindness, feeding difficulties and respiratory insufficiency may also be associated. There is evidence the disease is caused by homozygous or compound heterozygous mutation in the ASNS gene on chromosome 7q21.	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome (disorder)	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Huntington's chorea	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
A rare, severe early-onset neurodegenerative encephalopathy characterized mainly by developmental delay (DD) / developmental regression (DR), epilepsy, cortical atrophy, secondary hypomyelination and thin corpus callosum. Additional features include secondary microcephaly, hypotonia, spasticity, optic atrophy and skeletal anomalies.	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
A rare genetic disease characterised by infantile onset of severe inflammatory bowel disease manifesting with bloody diarrhoea and failure to thrive, and central nervous system disease with global developmental delay and regression, impaired speech, hypotonia, hyperreflexia, and epilepsy. Brain imaging shows global cerebral atrophy, thin corpus callosum, delayed myelination, and posterior leucoencephalopathy. Cases with recurrent infections and impaired T-cell responses to stimulation, as well as decreased T-cell subsets, have been reported.	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Progressive cerebello-cerebral atrophy (disorder)	Is a	True	Cerebral atrophy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
NAD(P)HX dehydratase deficiency	Is a	True	Cerebral atrophy (disorder)	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
415873013	Cerebral atrophy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
672059015	Cerebral atrophy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
415873013	Cerebral atrophy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
415873013	Cerebral atrophy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
672059015	Cerebral atrophy (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
672059015	Cerebral atrophy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
960451000195115	atrofia cerebrale	it	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
173061000077110	atrophie cérébrale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
173061000077110	atrophie cérébrale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
960451000195115	atrofia cerebrale	it	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module