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711406009: Autosomal recessive axonal neuropathy with neuromyotonia (disorder)


Status: current, Primitive. Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3078312013 Autosomal recessive axonal neuropathy with neuromyotonia en Synonym Active Case insensitive SNOMED CT core
3078319016 Autosomal recessive neuromyotonia with axonal neuropathy en Synonym Active Case insensitive SNOMED CT core
3078377011 Autosomal recessive axonal neuropathy with neuromyotonia (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3078517018 Myokymia, myotonia and muscle wasting en Synonym Active Case insensitive SNOMED CT core
3078521013 Gamstorp-Wohlfart syndrome en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive axonal neuropathy with neuromyotonia Finding site Axon structure true Inferred relationship Some 2
Autosomal recessive axonal neuropathy with neuromyotonia Is a Axonal neuropathy false Inferred relationship Some
Autosomal recessive axonal neuropathy with neuromyotonia Is a Neuromyotonia true Inferred relationship Some
Autosomal recessive axonal neuropathy with neuromyotonia Is a Hereditary disorder of nervous system true Inferred relationship Some
Autosomal recessive axonal neuropathy with neuromyotonia Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Autosomal recessive axonal neuropathy with neuromyotonia Finding site Peripheral nerve structure true Inferred relationship Some 1
Autosomal recessive axonal neuropathy with neuromyotonia Is a Peripheral axonal neuropathy true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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