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


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

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 SNOMED CT core module
1777611019 Charcot-Marie-Tooth disease, type I en Synonym Active Entire term case sensitive SNOMED CT core module
1786062015 Hereditary sensory-motor neuropathy, type I en Synonym Active Only initial character case insensitive SNOMED CT core module
1786063013 Peroneal muscular atrophy of demyelinating type en Synonym Active Entire term case insensitive SNOMED CT core module
1786064019 Inherited dominant hypertrophic neuropathy en Synonym Active Entire term case insensitive SNOMED CT core module
1786065018 Hereditary motor and sensory neuropathy type I en Synonym Active Only initial character case insensitive SNOMED CT core module
1786066017 Charcot-Marie-Tooth disease of demyelinating type en Synonym Active Entire term case sensitive SNOMED CT core module
1786067014 HSMN, type I en Synonym Active Entire term case sensitive SNOMED CT core module
2966574017 Charcot Marie Tooth disease, type 1 en Synonym Active Entire term case sensitive SNOMED CT core module


7 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Charcot-Marie-Tooth disease, type I Is a Charcot-Marie-Tooth disease false Inferred relationship Existential restriction modifier
Charcot-Marie-Tooth disease, type I Finding site Peripheral nervous system structure true Inferred relationship Existential restriction modifier 1
Charcot-Marie-Tooth disease, type I Associated morphology Neuropathic atrophy false Inferred relationship Existential restriction modifier 1
Charcot-Marie-Tooth disease, type I Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Charcot-Marie-Tooth disease, type I Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Charcot-Marie-Tooth disease, type I Associated morphology Neuropathic atrophy false Inferred relationship Existential restriction modifier 1
Charcot-Marie-Tooth disease, type I Is a Hereditary motor and sensory neuropathy true Inferred relationship Existential restriction modifier
Charcot-Marie-Tooth disease, type I Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Charcot-Marie-Tooth disease, type IA Is a True Charcot-Marie-Tooth disease, type I Inferred relationship Existential restriction modifier
Charcot-Marie-Tooth disease, type IC Is a True Charcot-Marie-Tooth disease, type I Inferred relationship Existential restriction modifier
Charcot-Marie-Tooth disease, type IB Is a True Charcot-Marie-Tooth disease, type I Inferred relationship Existential restriction modifier
Charcot-Marie-Tooth disease type IE Is a True Charcot-Marie-Tooth disease, type I Inferred relationship Existential restriction modifier
Charcot-Marie-Tooth disease type ID Is a True Charcot-Marie-Tooth disease, type I Inferred relationship Existential restriction modifier
Charcot-Marie-Tooth disease type IF Is a True Charcot-Marie-Tooth disease, type I Inferred relationship Existential restriction modifier
Peripheral myelin protein 2-related Charcot-Marie-Tooth disease type 1 Is a True Charcot-Marie-Tooth disease, type I Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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