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766934006: Isolated unilateral hemispheric cerebellar hypoplasia (disorder)


Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3663218018 Isolated unilateral hemispheric cerebellar hypoplasia (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3663220015 Isolated unilateral hemispheric cerebellar hypoplasia en Synonym Active Case insensitive SNOMED CT core
3663219014 A rare non-syndromic cerebellar malformation with characteristics of loss of volume in the right or left cerebellar hemisphere, with intact vermis and no other neurological anomalies (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. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Isolated unilateral hemispheric cerebellar hypoplasia Pathological process Pathological developmental process true Inferred relationship Some 1
Isolated unilateral hemispheric cerebellar hypoplasia Is a Finding of head region true Inferred relationship Some
Isolated unilateral hemispheric cerebellar hypoplasia Occurrence Congenital true Inferred relationship Some 1
Isolated unilateral hemispheric cerebellar hypoplasia Associated morphology Hypoplasia true Inferred relationship Some 1
Isolated unilateral hemispheric cerebellar hypoplasia Finding site Cerebral hemisphere structure true Inferred relationship Some 1
Isolated unilateral hemispheric cerebellar hypoplasia Is a Congenital hypoplasia of cerebrum true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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