715666007: Charcot-Marie-Tooth disease type IE (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Ear and auditory finding (finding)\Disorder of auditory system\Auditory system hereditary disorder\Charcot-Marie-Tooth disease type IE (disorder)
\Ear and auditory finding (finding)\Disorder of auditory system\Hearing disorder\Hearing loss\Sensorineural hearing loss\Charcot-Marie-Tooth disease type IE (disorder)
\Ear and auditory finding (finding)\Hearing finding (finding)\Hearing disorder\Hearing loss\Sensorineural hearing loss\Charcot-Marie-Tooth disease type IE (disorder)

\Functional finding\Hearing finding (finding)\Hearing disorder\Hearing loss\Sensorineural hearing loss\Charcot-Marie-Tooth disease type IE (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy (disorder)\Charcot-Marie-Tooth disease, type I (disorder)\Charcot-Marie-Tooth disease type IE (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Auditory system hereditary disorder\Charcot-Marie-Tooth disease type IE (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Charcot-Marie-Tooth disease, type I (disorder)\Charcot-Marie-Tooth disease type IE (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy (disorder)\Charcot-Marie-Tooth disease, type I (disorder)\Charcot-Marie-Tooth disease type IE (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Auditory system hereditary disorder\Charcot-Marie-Tooth disease type IE (disorder)
\Disease\Disorder of body system\Disorder of auditory system\Auditory system hereditary disorder\Charcot-Marie-Tooth disease type IE (disorder)
\Disease\Disorder of body system\Disorder of auditory system\Hearing disorder\Hearing loss\Sensorineural hearing loss\Charcot-Marie-Tooth disease type IE (disorder)
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy (disorder)\Charcot-Marie-Tooth disease, type I (disorder)\Charcot-Marie-Tooth disease type IE (disorder)
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the peripheral nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy (disorder)\Charcot-Marie-Tooth disease, type I (disorder)\Charcot-Marie-Tooth disease type IE (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Charcot-Marie-Tooth disease type IE (disorder)	Is a	Auditory system hereditary disorder	true	Inferred relationship	Some
Charcot-Marie-Tooth disease type IE (disorder)	Is a	Charcot-Marie-Tooth disease, type I (disorder)	true	Inferred relationship	Some
Charcot-Marie-Tooth disease type IE (disorder)	Finding site	Peripheral nervous system structure	true	Inferred relationship	Some	2
Charcot-Marie-Tooth disease type IE (disorder)	Finding site	Structure of auditory system (body structure)	true	Inferred relationship	Some	1
Charcot-Marie-Tooth disease type IE (disorder)	Is a	Sensorineural hearing loss	true	Inferred relationship	Some
Charcot-Marie-Tooth disease type IE (disorder)	Interprets	Hearing	true	Inferred relationship	Some	3

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3303350014	Charcot-Marie-Tooth disease and deafness	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3303351013	Charcot-Marie-Tooth disease type IE (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3303352018	Charcot-Marie-Tooth disease type IE	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3303353011	Charcot-Marie-Tooth disease type 1E	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5858031000172114	maladie de Charcot-Marie-Tooth type 1E	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
5092121000172117	CMT 1E	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)
5092131000172119	HMSN 1E	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)
5092141000172114	hereditaire motorische en sensorische neuropathie type 1E	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
5092151000172111	ziekte van Charcot-Marie-Tooth type 1E	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)