699866005: Progressive bulbar palsy with sensorineural deafness (disorder)

SNOMED CT Concept\Clinical finding\...

\Central nervous system finding\Finding of brain\Encephalopathy\Disorder of brain stem\Progressive bulbar palsy\Brown-Vialetto-Van Laere syndrome
\Central nervous system finding\Disorder of the central nervous system\Upper motor neuron disease\Progressive bulbar palsy\Brown-Vialetto-Van Laere syndrome
\Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Disorder of brain stem\Progressive bulbar palsy\Brown-Vialetto-Van Laere syndrome

\Finding of head and neck region\Head finding\...

\Finding of brain\Encephalopathy\Disorder of brain stem\Progressive bulbar palsy\Brown-Vialetto-Van Laere syndrome

\Finding of head region\Progressive bulbar palsy\Brown-Vialetto-Van Laere syndrome

\Disorder of head\Encephalopathy\Disorder of brain stem\Progressive bulbar palsy\Brown-Vialetto-Van Laere syndrome

\Ear and auditory finding\Disorder of auditory system\Auditory system hereditary disorder\Brown-Vialetto-Van Laere syndrome
\Ear and auditory finding\Disorder of auditory system\Hearing disorder\Hearing loss\Sensorineural hearing loss\Brown-Vialetto-Van Laere syndrome
\Ear and auditory finding\Hearing finding\Hearing disorder\Hearing loss\Sensorineural hearing loss\Brown-Vialetto-Van Laere syndrome

\Functional finding\Hearing finding\Hearing disorder\Hearing loss\Sensorineural hearing loss\Brown-Vialetto-Van Laere syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Brown-Vialetto-Van Laere syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Auditory system hereditary disorder\Brown-Vialetto-Van Laere syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Brown-Vialetto-Van Laere syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Brown-Vialetto-Van Laere syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Auditory system hereditary disorder\Brown-Vialetto-Van Laere syndrome
\Disease\Disorder of body system\Disorder of auditory system\Auditory system hereditary disorder\Brown-Vialetto-Van Laere syndrome
\Disease\Disorder of body system\Disorder of auditory system\Hearing disorder\Hearing loss\Sensorineural hearing loss\Brown-Vialetto-Van Laere syndrome
\Disease\Disorder of body system\Neurological disorder\Neuropathy\Disorder of cranial nerve\Multiple cranial nerve lesions and linked syndromes\Progressive bulbar palsy\Brown-Vialetto-Van Laere syndrome
\Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Brown-Vialetto-Van Laere syndrome
\Disease\Disorder of body system\Neurological disorder\Motor neurone disease\Upper motor neuron disease\Progressive bulbar palsy\Brown-Vialetto-Van Laere syndrome
\Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Upper motor neuron disease\Progressive bulbar palsy\Brown-Vialetto-Van Laere syndrome
\Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Disorder of brain stem\Progressive bulbar palsy\Brown-Vialetto-Van Laere syndrome
\Disease\Disorder of head\Encephalopathy\Disorder of brain stem\Progressive bulbar palsy\Brown-Vialetto-Van Laere syndrome

Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2986053017 Progressive bulbar palsy with sensorineural deafness (disorder) en Fully specified name Active Case insensitive SNOMED CT core

2986081011 Progressive bulbar palsy with sensorineural deafness en Synonym Active Case insensitive SNOMED CT core

2986109012 Brown-Vialetto-Van Laere syndrome en Synonym Active Case sensitive SNOMED CT core

2986122016 Pontobulbar palsy with deafness en Synonym Active Case insensitive SNOMED CT core

3881256019 Riboflavin transporter deficiency en Synonym Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Brown-Vialetto-Van Laere syndrome	Is a	Auditory system hereditary disorder	true	Inferred relationship	Some
Brown-Vialetto-Van Laere syndrome	Is a	Sensorineural hearing loss	true	Inferred relationship	Some
Brown-Vialetto-Van Laere syndrome	Finding site	Structure of auditory system	true	Inferred relationship	Some	2
Brown-Vialetto-Van Laere syndrome	Interprets	Hearing	true	Inferred relationship	Some	3
Brown-Vialetto-Van Laere syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Brown-Vialetto-Van Laere syndrome	Finding site	Structure of cranial nerve nucleus	true	Inferred relationship	Some	1
Brown-Vialetto-Van Laere syndrome	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Some
Brown-Vialetto-Van Laere syndrome	Is a	Progressive bulbar palsy	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
2986053017	Progressive bulbar palsy with sensorineural deafness (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
2986081011	Progressive bulbar palsy with sensorineural deafness	en	Synonym	Active	Case insensitive	SNOMED CT core
2986109012	Brown-Vialetto-Van Laere syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
2986122016	Pontobulbar palsy with deafness	en	Synonym	Active	Case insensitive	SNOMED CT core
3881256019	Riboflavin transporter deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core