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77097004: Oculopharyngeal muscular dystrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
127990018 Oculopharyngeal muscular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
127991019 Oculopharyngeal dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
817889017 Oculopharyngeal muscular dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
127990018 Oculopharyngeal muscular dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
127990018 Oculopharyngeal muscular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
127991019 Oculopharyngeal dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
127991019 Oculopharyngeal dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
817889017 Oculopharyngeal muscular dystrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
817889017 Oculopharyngeal muscular dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
572211000274117 Okulopharyngeale Muskeldystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
648331000274113 OPMD - Okulopharyngeale Muskeldystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
628971000172117 dystrophie musculaire oculopharyngée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
628971000172117 dystrophie musculaire oculopharyngée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
572211000274117 Okulopharyngeale Muskeldystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
648331000274113 OPMD - Okulopharyngeale Muskeldystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3440951001000117 Muskeldystrophie, okulopharyngeale 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
Oculopharyngeal muscular dystrophy Is a Disorder of orbit false Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Disorder of respiratory system false Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Disorder of upper digestive tract (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Disorder of digestive organ false Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Finding site Structure of extraocular muscle false Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculopharyngeal muscular dystrophy Finding site Muscle structure of pharynx false Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculopharyngeal muscular dystrophy Is a anomalie congénitale de l'appareil respiratoire false Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Pharyngeal paralysis false Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Myopathy of extraocular muscles true Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Oculopharyngeal muscular dystrophy Is a affection de l'oreille, du nez et de la gorge false Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Disorder of upper digestive tract (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Disorder of digestive organ false Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Pharyngeal paralysis false Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Associated morphology Dystrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculopharyngeal muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Oculopharyngeal muscular dystrophy Is a Disease of pharynx false Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Finding site Muscle structure of pharynx true Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculopharyngeal muscular dystrophy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculopharyngeal muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Oculopharyngeal muscular dystrophy Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Oculopharyngeal muscular dystrophy Finding site Structure of extraocular muscle false Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculopharyngeal muscular dystrophy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Oculopharyngeal muscular dystrophy Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Oculopharyngeal muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Oculopharyngeal muscular dystrophy Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Oculopharyngeal muscular dystrophy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 2
Oculopharyngeal muscular dystrophy Finding site Structure of extraocular muscle true Inferred relationship Existential restriction modifier (core metadata concept) 2
Oculopharyngeal muscular dystrophy Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Oculopharyngeal muscular dystrophy Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculopharyngeal muscular dystrophy Is a Congenital structural abnormality of orbit proper (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculopharyngeal muscular dystrophy Is a Congenital anomaly of pharynx true Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Chronic disease of respiratory system true Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Chronic digestive system disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Congenital anomaly of neck true Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Musculoskeletal disorder of the neck (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Chronic disease of ocular adnexa true Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a Congenital anomaly of ocular adnexa (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 3
Oculopharyngeal muscular dystrophy Is a Congenital anomaly of face (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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