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30508001: Charcot-Marie-Tooth disease, type II (disorder)


    Status: retired, 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
    51056015 Charcot-Marie-Tooth disease, type II en Synonym Active Entire term case sensitive SNOMED CT core module
    51057012 Hereditary sensory-motor neuropathy, type II en Synonym Active Only initial character case insensitive SNOMED CT core module
    51058019 Inherited neuronal peroneal muscular atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
    484605018 Charcot-Marie-Tooth disease of neuronal type en Synonym Active Entire term case sensitive SNOMED CT core module
    484606017 Autosomal recessive sensory neuropathy en Synonym Active Entire term case insensitive SNOMED CT core module
    484607014 Dominant hereditary sensory neuropathy, type II en Synonym Active Only initial character case insensitive SNOMED CT core module
    484608016 Hereditary sensory and autonomic neuropathy type II en Synonym Active Only initial character case insensitive SNOMED CT core module
    484609012 Peroneal muscular atrophy of neuronal type en Synonym Active Entire term case insensitive SNOMED CT core module
    484610019 Painless whitlow disease en Synonym Active Entire term case insensitive SNOMED CT core module
    484611015 Hereditary sensory and autonomic neuropathy, type II en Synonym Active Only initial character case insensitive SNOMED CT core module
    484612010 Hereditary motor and sensory neuropathy type II en Synonym Active Only initial character case insensitive SNOMED CT core module
    761520018 Charcot-Marie-Tooth disease, type II (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Charcot-Marie-Tooth disease, type II Is a Charcot-Marie-Tooth disease false Inferred relationship Existential restriction modifier
    Charcot-Marie-Tooth disease, type II Associated morphology Atrophy false Inferred relationship Existential restriction modifier 1
    Charcot-Marie-Tooth disease, type II Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
    Charcot-Marie-Tooth disease, type II Finding site Nerve structure false Inferred relationship Existential restriction modifier 1
    Charcot-Marie-Tooth disease, type II Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier
    Charcot-Marie-Tooth disease, type II Associated morphology Neuropathic atrophy false Inferred relationship Existential restriction modifier 2
    Charcot-Marie-Tooth disease, type II Is a Neuropathy false Inferred relationship Existential restriction modifier
    Charcot-Marie-Tooth disease, type II Associated morphology Atrophy false Inferred relationship Existential restriction modifier 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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