4183003: hereditaire motorische en sensorische neuropathie type 1C (aandoening)

SNOMED CT Concept\Clinical finding (finding)\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 IC (disorder)

\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Charcot-Marie-Tooth disease, type I (disorder)\Charcot-Marie-Tooth disease, type IC (disorder)

\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 IC (disorder)
\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 IC (disorder)
\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 IC (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

8465014 Charcot-Marie-Tooth disease, type IC en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

778663018 Charcot-Marie-Tooth disease, type IC (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

107471000146110 hereditaire motorische en sensorische neuropathie type 1C nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

922501000146114 hereditaire motorische en sensorische neuropathie type 1C (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

1273861000146118 HMSN 1C nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

1273871000146112 ziekte van Charcot-Marie-Tooth type 1C nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

1273881000146114 CMT 1C nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Charcot-Marie-Tooth disease, type IC (disorder)	Is a	Charcot-Marie-Tooth disease, type I	false	Inferred relationship	Some
Charcot-Marie-Tooth disease, type IC (disorder)	Finding site	Peripheral nervous system structure	true	Inferred relationship	Some	1
Charcot-Marie-Tooth disease, type IC (disorder)	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1
Charcot-Marie-Tooth disease, type IC (disorder)	Associated morphology	Atrophy	false	Inferred relationship	Some	1
Charcot-Marie-Tooth disease, type IC (disorder)	Associated morphology	Neuropathic atrophy	false	Inferred relationship	Some	1
Charcot-Marie-Tooth disease, type IC (disorder)	Finding site	Nerve structure	false	Inferred relationship	Some
Charcot-Marie-Tooth disease, type IC (disorder)	Is a	Charcot-Marie-Tooth disease, type I (disorder)	true	Inferred relationship	Some
Charcot-Marie-Tooth disease, type IC (disorder)	Associated morphology	Neuropathic atrophy	false	Inferred relationship	Some	1
Charcot-Marie-Tooth disease, type IC (disorder)	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1

Inbound Relationships

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Active

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Characteristic

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This concept is not in any reference sets