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764733009: Progressive external ophthalmoplegia, myopathy, emaciation syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3654902013 Progressive external ophthalmoplegia, myopathy, emaciation syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3654903015 Progressive external ophthalmoplegia, myopathy, emaciation syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3654905010 PEO (progressive external ophthalmoplegia) myopathy emaciation syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3654906011 Mitochondrial DNA (deoxyribonucleic acid) maintenance syndrome due to MGME1 (mitochondrial genome maintenance exonuclease 1) deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3654907019 A rare mitochondrial oxidative phosphorylation disorder due to nuclear deoxyribonucleic acid anomalies. The disease is characterised by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with generalised muscle wasting, profound emaciation, respiratory failure, spinal deformity and facial muscle weakness (manifesting with ptosis, dysphonia, dysphagia and nasal speech). Intellectual disability, gastrointestinal symptoms (nausea, abdominal fullness, and loss of appetite), dilated cardiomyopathy and renal colic have also been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3654908012 A rare mitochondrial oxidative phosphorylation disorder due to nuclear deoxyribonucleic acid anomalies. The disease is characterized by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with generalized muscle wasting, profound emaciation, respiratory failure, spinal deformity and facial muscle weakness (manifesting with ptosis, dysphonia, dysphagia and nasal speech). Intellectual disability, gastrointestinal symptoms (nausea, abdominal fullness, and loss of appetite), dilated cardiomyopathy and renal colic have also been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Is a Mitochondrial myopathy true Inferred relationship Some
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Is a Progressive external ophthalmoplegia true Inferred relationship Some
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Is a Metabolic encephalopathy true Inferred relationship Some
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Is a Congenital disease (disorder) true Inferred relationship Some
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Is a Hereditary disorder of nervous system true Inferred relationship Some
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Some
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Occurrence Congenital true Inferred relationship Some 3
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Finding site Skeletal muscle structure true Inferred relationship Some 3
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Finding site Brain structure true Inferred relationship Some 1
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Occurrence Congenital true Inferred relationship Some 1
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Occurrence Congenital true Inferred relationship Some 2
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Finding site Eye region structure (body structure) true Inferred relationship Some 2
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Is a Chronic brain syndrome true Inferred relationship Some
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Is a Myopathy of extraocular muscles true Inferred relationship Some
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Clinical course Progressive (qualifier value) true Inferred relationship Some 5
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Is a Chronic metabolic disorder true Inferred relationship Some
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Finding site Structure of extraocular muscle true Inferred relationship Some 4
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Interprets Movement true Inferred relationship Some 7
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Interprets Movement observable true Inferred relationship Some 6
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Has interpretation Absent true Inferred relationship Some 6

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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US English

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