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763829004: oculofaryngodistale myopathie (aandoening)


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
3644147018 Oculopharyngodistal myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3644148011 Oculopharyngeal distal myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3644149015 Oculopharyngodistal myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3644150015 OPDM - oculopharyngodistal myopathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6485391000146112 oculofaryngodistale myopathie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6485401000146110 oculofaryngodistale myopathie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7321311000146116 OPMD nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3644151016 A rare genetic neuromuscular disease with characteristics of progressive external ocular, facial and pharyngeal muscle weakness, leading to variable degrees of ptosis, ophthalmoparesis, facial muscle atrophy, dysarthria and dysphagia, as well as distal muscle weakness and atrophy of lower and upper extremities. Respiratory muscle involvement is common, but sensorineural hearing loss, asymmetrical extremity weakness and severe proximal weakness are rare. 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
Oculopharyngodistal myopathy (disorder) Is a Distal muscular dystrophy true Inferred relationship Some
Oculopharyngodistal myopathy (disorder) Is a Disorder of pharynx true Inferred relationship Some
Oculopharyngodistal myopathy (disorder) Is a Pharyngeal paresis true Inferred relationship Some
Oculopharyngodistal myopathy (disorder) Is a Congenital ptosis (disorder) false Inferred relationship Some
Oculopharyngodistal myopathy (disorder) Is a Digestive system hereditary disorder (disorder) true Inferred relationship Some
Oculopharyngodistal myopathy (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Some
Oculopharyngodistal myopathy (disorder) Occurrence Congenital false Inferred relationship Some 4
Oculopharyngodistal myopathy (disorder) Associated morphology Dystrophy true Inferred relationship Some 4
Oculopharyngodistal myopathy (disorder) Finding site Skeletal muscle structure true Inferred relationship Some 4
Oculopharyngodistal myopathy (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 4
Oculopharyngodistal myopathy (disorder) Finding site Upper eyelid structure true Inferred relationship Some 2
Oculopharyngodistal myopathy (disorder) Occurrence Congenital false Inferred relationship Some 1
Oculopharyngodistal myopathy (disorder) Associated morphology congenitale ptosis (afwijkende morfologie) false Inferred relationship Some 2
Oculopharyngodistal myopathy (disorder) Occurrence Congenital false Inferred relationship Some 3
Oculopharyngodistal myopathy (disorder) Occurrence Congenital false Inferred relationship Some 2
Oculopharyngodistal myopathy (disorder) Associated morphology Dystrophy false Inferred relationship Some 1
Oculopharyngodistal myopathy (disorder) Finding site Muscle structure of pharynx false Inferred relationship Some 3
Oculopharyngodistal myopathy (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 1
Oculopharyngodistal myopathy (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 1
Oculopharyngodistal myopathy (disorder) Is a Ptosis of eyelid true Inferred relationship Some
Oculopharyngodistal myopathy (disorder) Finding site Muscle structure of pharynx true Inferred relationship Some 3
Oculopharyngodistal myopathy (disorder) Is a Chronic disease of respiratory system true Inferred relationship Some
Oculopharyngodistal myopathy (disorder) Is a Chronic digestive system disorder true Inferred relationship Some
Oculopharyngodistal myopathy (disorder) Is a Chronic disease of ocular adnexa true Inferred relationship Some
Oculopharyngodistal myopathy (disorder) Is a Chronic disease of musculoskeletal system false Inferred relationship Some
Oculopharyngodistal myopathy (disorder) Associated morphology Prolapse (morphologic abnormality) true Inferred relationship Some 2
Oculopharyngodistal myopathy (disorder) Is a Musculoskeletal disorder of the neck false Inferred relationship Some
Oculopharyngodistal myopathy (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Oculopharyngodistal myopathy (disorder) Is a Cervical myopathy (disorder) true Inferred relationship Some
Oculopharyngodistal myopathy (disorder) Interprets Movement true Inferred relationship Some 5
Oculopharyngodistal myopathy (disorder) Is a Movement disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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