720506002: Deafness and myopia syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of head and neck region\Head finding\Finding of head region\Ear finding\Disorder of ear\Deafness and myopia syndrome
\Finding of head and neck region\Head finding\Disorder of head\Disorder of ear\Deafness and myopia syndrome
\Finding of head and neck region\Ear, nose and throat finding\Ear finding\Disorder of ear\Deafness and myopia syndrome
\Finding of head and neck region\Ear, nose and throat finding\Ear, nose and throat disorder\Disorder of ear\Deafness and myopia syndrome

\Ear and auditory finding\Disorder of auditory system\Auditory system hereditary disorder\Deafness and myopia syndrome
\Ear and auditory finding\Disorder of auditory system\Hearing disorder\Hearing loss\Hearing loss associated with syndrome\Deafness and myopia syndrome
\Ear and auditory finding\Disorder of auditory system\Disorder of ear\Deafness and myopia syndrome
\Ear and auditory finding\Ear finding\Disorder of ear\Deafness and myopia syndrome
\Ear and auditory finding\Hearing finding\Hearing disorder\Hearing loss\Hearing loss associated with syndrome\Deafness and myopia syndrome

\Eye / vision finding\Visual system disorder\...

\Hereditary disorder of the visual system\Deafness and myopia syndrome

\Disorder of vision\Disorder of refraction AND/OR accommodation\Disorder of refraction\Myopia\Severe myopia\Deafness and myopia syndrome

\Functional finding\Hearing finding\Hearing disorder\Hearing loss\Hearing loss associated with syndrome\Deafness and myopia syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the visual system\Deafness and myopia syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Auditory system hereditary disorder\Deafness and myopia syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Deafness and myopia syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the visual system\Deafness and myopia syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Auditory system hereditary disorder\Deafness and myopia syndrome
\Disease\Disorder of body system\Disorder of auditory system\Auditory system hereditary disorder\Deafness and myopia syndrome
\Disease\Disorder of body system\Disorder of auditory system\Hearing disorder\Hearing loss\Hearing loss associated with syndrome\Deafness and myopia syndrome
\Disease\Disorder of body system\Disorder of auditory system\Disorder of ear\Deafness and myopia syndrome
\Disease\Disorder of body system\Visual system disorder\Hereditary disorder of the visual system\Deafness and myopia syndrome
\Disease\Disorder of body system\Visual system disorder\Disorder of vision\Disorder of refraction AND/OR accommodation\Disorder of refraction\Myopia\Severe myopia\Deafness and myopia syndrome
\Disease\Ear, nose and throat disorder\Disorder of ear\Deafness and myopia syndrome
\Disease\Disorder of head\Disorder of ear\Deafness and myopia syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3321066016 Deafness and myopia syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3321067013 Deafness and myopia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

3321068015 High myopia and sensorineural deafness en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Deafness and myopia syndrome	Is a	Severe myopia	true	Inferred relationship	Existential restriction modifier
Deafness and myopia syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Deafness and myopia syndrome	Is a	Hearing loss associated with syndrome	true	Inferred relationship	Existential restriction modifier
Deafness and myopia syndrome	Is a	Auditory system hereditary disorder	true	Inferred relationship	Existential restriction modifier
Deafness and myopia syndrome	Is a	Hereditary disorder of the visual system	true	Inferred relationship	Existential restriction modifier
Deafness and myopia syndrome	Finding site	Structure of visual system	true	Inferred relationship	Existential restriction modifier	2
Deafness and myopia syndrome	Finding site	Ear structure	true	Inferred relationship	Existential restriction modifier	1
Deafness and myopia syndrome	Interprets	Hearing, function	true	Inferred relationship	Existential restriction modifier	3
Deafness and myopia syndrome	Is a	Disorder of ear	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3321066016	Deafness and myopia syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3321067013	Deafness and myopia syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3321068015	High myopia and sensorineural deafness	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module