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787172004: Childhood-onset autosomal recessive myopathy with external ophthalmoplegia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3774798014 Childhood-onset autosomal recessive myopathy with external ophthalmoplegia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3774799018 Childhood-onset autosomal recessive myopathy with external ophthalmoplegia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3774802010 A rare genetic non-dystrophic myopathy disease with characteristics of childhood-onset severe external ophthalmoplegia, typically without ptosis, associated with mild, very slowly progressive muscular weakness and atrophy, involving the facial, neck flexor and limb muscles. Muscle biopsy shows type 1 fiber uniformity, absent or abnormally small type 2A fibers, increased variability of fiber size, internalized nuclei and/or fatty infiltration. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3774803017 A rare genetic non-dystrophic myopathy disease with characteristics of childhood-onset severe external ophthalmoplegia, typically without ptosis, associated with mild, very slowly progressive muscular weakness and atrophy, involving the facial, neck flexor and limb muscles. Muscle biopsy shows type 1 fibre uniformity, absent or abnormally small type 2A fibres, increased variability of fibre size, internalised nuclei and/or fatty infiltration. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3774798014 Childhood-onset autosomal recessive myopathy with external ophthalmoplegia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3774799018 Childhood-onset autosomal recessive myopathy with external ophthalmoplegia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3774802010 A rare genetic non-dystrophic myopathy disease with characteristics of childhood-onset severe external ophthalmoplegia, typically without ptosis, associated with mild, very slowly progressive muscular weakness and atrophy, involving the facial, neck flexor and limb muscles. Muscle biopsy shows type 1 fiber uniformity, absent or abnormally small type 2A fibers, increased variability of fiber size, internalized nuclei and/or fatty infiltration. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3774803017 A rare genetic non-dystrophic myopathy disease with characteristics of childhood-onset severe external ophthalmoplegia, typically without ptosis, associated with mild, very slowly progressive muscular weakness and atrophy, involving the facial, neck flexor and limb muscles. Muscle biopsy shows type 1 fibre uniformity, absent or abnormally small type 2A fibres, increased variability of fibre size, internalised nuclei and/or fatty infiltration. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3412911001000112 Im Kindesalter beginnende autosomal-rezessive Myopathie mit externer Ophtalmoplegie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5797211000241114 myopathie autosomique récessive avec ophtalmoplégie externe débutant dans l'enfance fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5797211000241114 myopathie autosomique récessive avec ophtalmoplégie externe débutant dans l'enfance fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3412911001000112 Im Kindesalter beginnende autosomal-rezessive Myopathie mit externer Ophtalmoplegie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Is a Hereditary disorder of nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Occurrence Childhood true Inferred relationship Existential restriction modifier (core metadata concept) 2
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Is a Chronic nervous system disorder (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Is a Chronic disease of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept)
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Is a External ophthalmoplegia (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Is a Myoneural disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Occurrence Childhood true Inferred relationship Existential restriction modifier (core metadata concept) 3
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Occurrence Childhood true Inferred relationship Existential restriction modifier (core metadata concept) 1
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Finding site Eye region structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Finding site Peripheral nervous system structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 4
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Is a Progressive external ophthalmoplegia true Inferred relationship Existential restriction modifier (core metadata concept)
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Finding site Structure of extraocular muscle true Inferred relationship Existential restriction modifier (core metadata concept) 5
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Is a Myopathy of extraocular muscles true Inferred relationship Existential restriction modifier (core metadata concept)
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 7
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Interprets Movement observable true Inferred relationship Existential restriction modifier (core metadata concept) 6
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Has interpretation Absent true Inferred relationship Existential restriction modifier (core metadata concept) 6

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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