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1144427006: Diffuse atrophy of cerebrum (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2025. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4541924012 Diffuse atrophy of cerebrum (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4541925013 Diffuse atrophy of cerebrum en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4542682013 Diffuse atrophy of cerebral structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Diffuse atrophy of cerebrum (disorder) Is a Cerebral atrophy true Inferred relationship Some
Diffuse atrophy of cerebrum (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 Some 1
Diffuse atrophy of cerebrum (disorder) Associated morphology Diffuse atrophy true Inferred relationship Some 1
Diffuse atrophy of cerebrum (disorder) Is a Global brain atrophy (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
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 Diffuse atrophy of cerebrum (disorder) Inferred relationship Some
A rare, genetic, central nervous system malformation syndrome characterized by congenital, progressive microcephaly, neonatal to infancy-onset of severe, intractable seizures, and diffuse cerebral cortex and cerebellar vermis atrophy with mild cerebellar hemisphere atrophy, associated with profound global developmental delay. Hypotonia or hypertonia with brisk reflexes, variable dysmorphic facial features, ophthalmological signs (cortical visual impairment, nystagmus, eye deviation) and episodes of sudden extreme agitation caused by severe illness may also be associated. Is a True Diffuse atrophy of cerebrum (disorder) Inferred relationship Some

This concept is not in any reference sets

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