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1144337000: Congenital hypoplasia of cerebral hemisphere (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
4541654016 Congenital hypoplasia of cerebral hemisphere en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4541655015 Congenital hypoplasia of cerebral hemisphere (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5449596013 Hemispheric cerebral hypoplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


8 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hypoplasia of cerebral hemisphere Is a Finding of head region true Inferred relationship Some
Congenital hypoplasia of cerebral hemisphere Is a Congenital hypoplasia of cerebrum true Inferred relationship Some
Congenital hypoplasia of cerebral hemisphere Occurrence Congenital true Inferred relationship Some 1
Congenital hypoplasia of cerebral hemisphere Finding site Cerebral hemisphere structure (body structure) true Inferred relationship Some 1
Congenital hypoplasia of cerebral hemisphere Associated morphology Hypoplasia true Inferred relationship Some 1
Congenital hypoplasia of cerebral hemisphere Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital hypoplasia of cerebral white matter (disorder) Is a True Congenital hypoplasia of cerebral hemisphere Inferred relationship Some
Congenital hypoplasia of frontal lobe (disorder) Is a True Congenital hypoplasia of cerebral hemisphere Inferred relationship Some
Isolated bilateral hemispheric cerebellar hypoplasia is a rare cerebellar malformation characterized by hypoplasia of both cerebellar hemispheres with no other cerebellar/cerebral anomaly or other associated clinical feature. Affected patients present with mild hypotonia with motor delay, mild cognitive impairment, language delay, visuospatial and verbal memory deficits, dysdiadochokinesis, intentional tremor, and possible presence of emotional fragility and mild depression. Is a False Congenital hypoplasia of cerebral hemisphere Inferred relationship Some
Isolated unilateral hemispheric cerebellar hypoplasia is a rare, non-syndromic cerebellar malformation characterized by loss of volume in the right or left cerebellar hemisphere, with intact vermis and no other neurological anomalies (i.e. normal cerebral hemispheres, fourth ventricle, pons, medulla and midbrain). Patients may be asymptomatic or may present developmental and speech delay, hypotonia, abnormal ocular movements, persistent headaches and/or peripheral vertigo and ataxia. Neurological examination is otherwise normal. Is a False Congenital hypoplasia of cerebral hemisphere Inferred relationship Some
Congenital hypoplasia of olfactory tract (disorder) Is a True Congenital hypoplasia of cerebral hemisphere Inferred relationship Some

This concept is not in any reference sets

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