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128202008: Hereditary motor and sensory neuropathy (disorder)

    Status: retired, 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
    206429016 Hereditary sensory-motor neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    206430014 Hereditary sensory and motor neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    206431013 Hereditary sensorimotor neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    206432018 HSMN en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    206433011 HMSN en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    206434017 Hereditary motor and sensory neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    474337018 Hereditary peripheral neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    474338011 CMT - Charcot-Marie-Tooth disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    474339015 HSMN - Hereditary sensory and motor neuropathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    474340018 HMSN - Hereditary motor and sensory neuropathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    474341019 Charcot-Marie-Tooth disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    474342014 Peroneal muscular atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    732167016 Hereditary motor and sensory neuropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    206429016 Hereditary sensory-motor neuropathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    206429016 Hereditary sensory-motor neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    206430014 Hereditary sensory and motor neuropathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    206430014 Hereditary sensory and motor neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    206431013 Hereditary sensorimotor neuropathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    206431013 Hereditary sensorimotor neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    206432018 HSMN en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    206433011 HMSN en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    206434017 Hereditary motor and sensory neuropathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    206434017 Hereditary motor and sensory neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    474337018 Hereditary peripheral neuropathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    474337018 Hereditary peripheral neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    474338011 CMT - Charcot-Marie-Tooth disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    474339015 HSMN - Hereditary sensory and motor neuropathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    474340018 HMSN - Hereditary motor and sensory neuropathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    474341019 Charcot-Marie-Tooth disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    474342014 Peroneal muscular atrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    474342014 Peroneal muscular atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    732167016 Hereditary motor and sensory neuropathy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    732167016 Hereditary motor and sensory neuropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) 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 Existential restriction modifier (core metadata concept)
    Hereditary motor and sensory neuropathy Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group
    X-linked hereditary motor and sensory neuropathy Is a False Hereditary motor and sensory neuropathy Inferred relationship Existential restriction modifier (core metadata concept)
    Déjérine-Sottas disease Is a False Hereditary motor and sensory neuropathy Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary sensory neuropathy (disorder) Is a False Hereditary motor and sensory neuropathy Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary motor and sensory neuropathy with optic atrophy Is a False Hereditary motor and sensory neuropathy Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary motor and sensory neuropathy with retinitis pigmentosa (disorder) Is a False Hereditary motor and sensory neuropathy Inferred relationship Existential restriction modifier (core metadata concept)
    Phytanic acid storage disease (disorder) Is a False Hereditary motor and sensory neuropathy Inferred relationship Existential restriction modifier (core metadata concept)
    Charcot-Marie-Tooth disease Is a False Hereditary motor and sensory neuropathy Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary sensory-motor neuropathy, type V Is a False Hereditary motor and sensory neuropathy Inferred relationship Existential restriction modifier (core metadata concept)
    Peroneal muscular atrophy NOS Is a False Hereditary motor and sensory neuropathy Inferred relationship Existential restriction modifier (core metadata concept)

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

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