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50548001: Charcot-Marie-Tooth disease (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    84200019 Peroneal muscular atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
    84201015 Charcot-Marie-Tooth disease en Synonym Active Entire term case sensitive SNOMED CT core module
    495705018 CMT - Charcot-Marie-Tooth disease en Synonym Active Entire term case sensitive SNOMED CT core module
    788348015 Charcot-Marie-Tooth disease (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 Is a Muscle atrophy false Inferred relationship Existential restriction modifier
    Charcot-Marie-Tooth disease Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
    Charcot-Marie-Tooth disease Is a Hereditary motor and sensory neuropathy false Inferred relationship Existential restriction modifier
    Charcot-Marie-Tooth disease Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier
    Charcot-Marie-Tooth disease Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
    Charcot-Marie-Tooth disease Associated morphology Atrophy false Inferred relationship Existential restriction modifier 1
    Charcot-Marie-Tooth disease Associated morphology Neuropathic atrophy false Inferred relationship Existential restriction modifier 1
    Charcot-Marie-Tooth disease Is a Combined disorder of muscle AND peripheral nerve false Inferred relationship Existential restriction modifier
    Charcot-Marie-Tooth disease Is a Hereditary motor and sensory neuropathy false Inferred relationship Existential restriction modifier
    Charcot-Marie-Tooth disease Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
    Charcot-Marie-Tooth disease Associated morphology Neuropathic atrophy false Inferred relationship Existential restriction modifier 1

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Charcot-Marie-Tooth disease, type II Is a False Charcot-Marie-Tooth disease Inferred relationship Existential restriction modifier
    Charcot-Marie-Tooth disease, type I Is a False Charcot-Marie-Tooth disease Inferred relationship Existential restriction modifier
    Charcot-Marie-Tooth disease, type I Is a False Charcot-Marie-Tooth disease Inferred relationship Existential restriction modifier
    Charcot-Marie-Tooth disease, type II Is a False Charcot-Marie-Tooth disease Inferred relationship Existential restriction modifier
    Family history of Charcot-Marie-Tooth disease Associated finding False Charcot-Marie-Tooth disease Inferred relationship Existential restriction modifier 1
    Family history of Charcot-Marie-Tooth disease Associated finding False Charcot-Marie-Tooth disease Inferred relationship Existential restriction modifier 1
    Family history of Charcot-Marie-Tooth disease Associated finding False Charcot-Marie-Tooth disease Inferred relationship Existential restriction modifier 1

    This concept is not in any reference sets

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