722949001: Familial Ménière disease (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of head and neck region\Head finding\Finding of head region\Vestibular system finding\Labyrinthine disorder\Peripheral vertigo\Ménière's disease\Familial Ménière disease
\Finding of head and neck region\Head finding\Finding of head region\Ear finding\Disorder of ear\Disorder of inner ear\Labyrinthine disorder\Peripheral vertigo\Ménière's disease\Familial Ménière disease
\Finding of head and neck region\Head finding\Disorder of head\Disorder of ear\Disorder of inner ear\Labyrinthine disorder\Peripheral vertigo\Ménière's disease\Familial Ménière disease
\Finding of head and neck region\Ear, nose and throat finding\Ear finding\Disorder of ear\Disorder of inner ear\Labyrinthine disorder\Peripheral vertigo\Ménière's disease\Familial Ménière disease
\Finding of head and neck region\Ear, nose and throat finding\Ear, nose and throat disorder\Disorder of ear\Disorder of inner ear\Labyrinthine disorder\Peripheral vertigo\Ménière's disease\Familial Ménière disease

\Ear and auditory finding\Disorder of auditory system\Disorder of ear\Disorder of inner ear\Labyrinthine disorder\Peripheral vertigo\Ménière's disease\Familial Ménière disease
\Ear and auditory finding\Ear finding\Disorder of ear\Disorder of inner ear\Labyrinthine disorder\Peripheral vertigo\Ménière's disease\Familial Ménière disease

\Disease\Disorder of body system\Disorder of auditory system\Disorder of ear\Disorder of inner ear\Labyrinthine disorder\Peripheral vertigo\Ménière's disease\Familial Ménière disease
\Disease\Ear, nose and throat disorder\Disorder of ear\Disorder of inner ear\Labyrinthine disorder\Peripheral vertigo\Ménière's disease\Familial Ménière disease
\Disease\Disorder of head\Disorder of ear\Disorder of inner ear\Labyrinthine disorder\Peripheral vertigo\Ménière's disease\Familial Ménière disease
\Disease\Familial disease\Familial Ménière disease

Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3334418010 Familial Ménière disease (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

3334419019 Familial Ménière disease en Synonym Active Initial character case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial Ménière disease	Is a	Ménière's disease	true	Inferred relationship	Some
Familial Ménière disease	Is a	Familial disease	true	Inferred relationship	Some
Familial Ménière disease	Finding site	Labyrinth structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set