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128202008: Hereditary motor and sensory neuropathy (disorder)


    Status: retired, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    206429016 Hereditary sensory-motor neuropathy en Synonym Active Case insensitive SNOMED CT core
    206430014 Hereditary sensory and motor neuropathy en Synonym Active Case insensitive SNOMED CT core
    206431013 Hereditary sensorimotor neuropathy en Synonym Active Case insensitive SNOMED CT core
    206432018 HSMN en Synonym Active Case sensitive SNOMED CT core
    206433011 HMSN en Synonym Active Case sensitive SNOMED CT core
    206434017 Hereditary motor and sensory neuropathy en Synonym Active Case insensitive SNOMED CT core
    474337018 Hereditary peripheral neuropathy en Synonym Active Case insensitive SNOMED CT core
    474338011 CMT - Charcot-Marie-Tooth disease en Synonym Active Case sensitive SNOMED CT core
    474339015 HSMN - Hereditary sensory and motor neuropathy en Synonym Active Case sensitive SNOMED CT core
    474340018 HMSN - Hereditary motor and sensory neuropathy en Synonym Active Case sensitive SNOMED CT core
    474341019 Charcot-Marie-Tooth disease en Synonym Active Case sensitive SNOMED CT core
    474342014 Peroneal muscular atrophy en Synonym Active Case insensitive SNOMED CT core
    732167016 Hereditary motor and sensory neuropathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Hereditary motor and sensory neuropathy Is a Hereditary peripheral neuropathy false Inferred relationship Some
    Hereditary motor and sensory neuropathy Finding site Peripheral nervous system structure false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Hereditary motor and sensory neuropathy with optic atrophy Is a False Hereditary motor and sensory neuropathy Inferred relationship Some
    Hereditary motor and sensory neuropathy with retinitis pigmentosa Is a False Hereditary motor and sensory neuropathy Inferred relationship Some
    Phytanic acid storage disease Is a False Hereditary motor and sensory neuropathy Inferred relationship Some
    Charcot-Marie-Tooth disease Is a False Hereditary motor and sensory neuropathy Inferred relationship Some
    Hereditary sensory-motor neuropathy, type V Is a False Hereditary motor and sensory neuropathy Inferred relationship Some
    Peroneal muscular atrophy NOS Is a False Hereditary motor and sensory neuropathy Inferred relationship Some
    X-linked hereditary motor and sensory neuropathy Is a False Hereditary motor and sensory neuropathy Inferred relationship Some
    Déjérine-Sottas disease Is a False Hereditary motor and sensory neuropathy Inferred relationship Some
    Hereditary sensory neuropathy Is a False Hereditary motor and sensory neuropathy Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

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