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827117008: Autosomal recessive progressive external ophthalmoplegia (disorder)


Status: current, Primitive. Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3873907011 Autosomal recessive progressive external ophthalmoplegia en Synonym Active Case insensitive SNOMED CT core
3873908018 Autosomal recessive progressive external ophthalmoplegia (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3873909014 arPEO- autosomal recessive progressive external ophthalmoplegia en Synonym Active Case sensitive SNOMED CT core
3873910016 A rare genetic neuro-ophthalmological disease with characteristics of progressive weakness of the external eye muscles, resulting in bilateral ptosis and diffuse, symmetric ophthalmoparesis. Additional signs may include generalised skeletal muscle weakness, muscle atrophy, sensory axonal neuropathy, ataxia, cardiomyopathy, and psychiatric symptoms. It is usually more severe than autosomal dominant form. en Definition Active Case sensitive SNOMED CT core
3873911017 A rare genetic neuro-ophthalmological disease with characteristics of progressive weakness of the external eye muscles, resulting in bilateral ptosis and diffuse, symmetric ophthalmoparesis. Additional signs may include generalized skeletal muscle weakness, muscle atrophy, sensory axonal neuropathy, ataxia, cardiomyopathy, and psychiatric symptoms. It is usually more severe than autosomal dominant form. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive progressive external ophthalmoplegia Is a Hereditary disorder of the visual system true Inferred relationship Some
Autosomal recessive progressive external ophthalmoplegia Is a Progressive external ophthalmoplegia true Inferred relationship Some
Autosomal recessive progressive external ophthalmoplegia Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Autosomal recessive progressive external ophthalmoplegia Is a Hereditary disorder of nervous system true Inferred relationship Some
Autosomal recessive progressive external ophthalmoplegia Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Autosomal recessive progressive external ophthalmoplegia Is a Chronic metabolic disorder true Inferred relationship Some
Autosomal recessive progressive external ophthalmoplegia Is a Mitochondrial cytopathy true Inferred relationship Some
Autosomal recessive progressive external ophthalmoplegia Clinical course Progressive true Inferred relationship Some 1
Autosomal recessive progressive external ophthalmoplegia Finding site Structure of nervous system true Inferred relationship Some 2
Autosomal recessive progressive external ophthalmoplegia Finding site Structure of extraocular muscle true Inferred relationship Some 3
Autosomal recessive progressive external ophthalmoplegia Interprets Movement true Inferred relationship Some 5
Autosomal recessive progressive external ophthalmoplegia Interprets Movement observable true Inferred relationship Some 4
Autosomal recessive progressive external ophthalmoplegia Has interpretation Absent true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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