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770630005: Distal hereditary motor neuropathy type 1 (disorder)


Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3701703015 Distal hereditary motor neuropathy type 1 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3701704014 Distal hereditary motor neuropathy type 1 en Synonym Active Case insensitive SNOMED CT core
3701705010 Autosomal dominant distal juvenile spinal muscular atrophy type 1 en Synonym Active Case insensitive SNOMED CT core
3701706011 A rare neuromuscular disease with characteristics of slowly progressive lower limb muscular weakness and atrophy, without sensory impairment. Additional clinical features may include pes cavus, hammertoe and increased muscle tone. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Distal hereditary motor neuropathy type 1 Finding site Peripheral nervous system structure true Inferred relationship Some 2
Distal hereditary motor neuropathy type 1 Finding site Nerve structure true Inferred relationship Some 3
Distal hereditary motor neuropathy type 1 Is a Autosomal dominant distal hereditary motor neuropathy true Inferred relationship Some
Distal hereditary motor neuropathy type 1 Finding site Structure of nervous system false Inferred relationship Some 2
Distal hereditary motor neuropathy type 1 Is a Distal spinal muscular atrophy true Inferred relationship Some
Distal hereditary motor neuropathy type 1 Clinical course Progressive true Inferred relationship Some 1
Distal hereditary motor neuropathy type 1 Is a Chronic nervous system disorder true Inferred relationship Some
Distal hereditary motor neuropathy type 1 Is a Autosomal dominant hereditary disorder false 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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