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398040009: Charcot-Marie-Tooth disease, type I (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1765959019 Charcot-Marie-Tooth disease, type I (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1777611019 Charcot-Marie-Tooth disease, type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1786062015 Hereditary sensory-motor neuropathy, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786063013 Peroneal muscular atrophy of demyelinating type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786064019 Inherited dominant hypertrophic neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786065018 Hereditary motor and sensory neuropathy type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786066017 Charcot-Marie-Tooth disease of demyelinating type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1786067014 HSMN, type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2966574017 Charcot Marie Tooth disease, type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1765959019 Charcot-Marie-Tooth disease, type I (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1777611019 Charcot-Marie-Tooth disease, type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1786062015 Hereditary sensory-motor neuropathy, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786063013 Peroneal muscular atrophy of demyelinating type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786063013 Peroneal muscular atrophy of demyelinating type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786064019 Inherited dominant hypertrophic neuropathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786064019 Inherited dominant hypertrophic neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786065018 Hereditary motor and sensory neuropathy type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786066017 Charcot-Marie-Tooth disease of demyelinating type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1786067014 HSMN, type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2966574017 Charcot Marie Tooth disease, type 1 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2966574017 Charcot Marie Tooth disease, type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3408851001000119 Charcot-Marie-Tooth-Krankheit Typ 1 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3386401010 neuropathie sensitivo-motrice héréditaire de type I fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
368251000172118 neuropathie sensitivomotrice héréditaire type 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
617961000172116 neuropathie sensitivomotrice héréditaire de type I fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3386401010 neuropathie sensitivo-motrice héréditaire de type I fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
368251000172118 neuropathie sensitivomotrice héréditaire type 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
617961000172116 neuropathie sensitivomotrice héréditaire de type I fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3408851001000119 Charcot-Marie-Tooth-Krankheit Typ 1 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

7 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Charcot-Marie-Tooth disease, type I (disorder) Is a Charcot-Marie-Tooth disease false Inferred relationship Existential restriction modifier (core metadata concept)
Charcot-Marie-Tooth disease, type I (disorder) Finding site Peripheral nervous system structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Charcot-Marie-Tooth disease, type I (disorder) Associated morphology Neuropathic atrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Charcot-Marie-Tooth disease, type I (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Charcot-Marie-Tooth disease, type I (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Charcot-Marie-Tooth disease, type I (disorder) Associated morphology Neuropathic atrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Charcot-Marie-Tooth disease, type I (disorder) Is a Hereditary motor and sensory neuropathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Charcot-Marie-Tooth disease, type I (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Charcot-Marie-Tooth disease, type IA Is a True Charcot-Marie-Tooth disease, type I (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Charcot-Marie-Tooth disease, type IC (disorder) Is a True Charcot-Marie-Tooth disease, type I (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Charcot-Marie-Tooth disease, type IB Is a True Charcot-Marie-Tooth disease, type I (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Charcot-Marie-Tooth disease type IE (disorder) Is a True Charcot-Marie-Tooth disease, type I (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Charcot-Marie-Tooth disease type ID (disorder) Is a True Charcot-Marie-Tooth disease, type I (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Charcot-Marie-Tooth disease type IF Is a True Charcot-Marie-Tooth disease, type I (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Peripheral myelin protein 2-related Charcot-Marie-Tooth disease type 1 (disorder) Is a True Charcot-Marie-Tooth disease, type I (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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