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30767006: Gait apraxia (finding)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
484698013 Gait apraxia en Synonym Active Case insensitive SNOMED CT core
484699017 Apraxic gait en Synonym Active Case insensitive SNOMED CT core
51498014 Bruns' apraxia of gait en Synonym Active Case sensitive SNOMED CT core
761812013 Gait apraxia (finding) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Gait apraxia Is a High level sensorimotor gait disorder true Inferred relationship Some
Gait apraxia Is a Apraxia true Inferred relationship Some
Gait apraxia Interprets Nervous system function false Inferred relationship Some
Gait apraxia Interprets Functional observable false Inferred relationship Some
Gait apraxia Interprets Walking true Inferred relationship Some 2
Gait apraxia Interprets Gait observable true Inferred relationship Some 1
Gait apraxia Finding site Structure of lower limb false Inferred relationship Some
Gait apraxia Finding site Structure of nervous system false Inferred relationship Some
Gait apraxia Finding site Structure of musculoskeletal system true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Queensland allied health clinical finding reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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