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763829004: Oculopharyngodistal myopathy (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3644147018 Oculopharyngodistal myopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3644148011 Oculopharyngeal distal myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
3644149015 Oculopharyngodistal myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
3644150015 OPDM - oculopharyngodistal myopathy en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Oculopharyngodistal myopathy Is a Distal muscular dystrophy true Inferred relationship Existential restriction modifier
Oculopharyngodistal myopathy Is a Disorder of pharynx true Inferred relationship Existential restriction modifier
Oculopharyngodistal myopathy Is a Pharyngeal paresis true Inferred relationship Existential restriction modifier
Oculopharyngodistal myopathy Is a Congenital ptosis false Inferred relationship Existential restriction modifier
Oculopharyngodistal myopathy Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Oculopharyngodistal myopathy Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Oculopharyngodistal myopathy Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Oculopharyngodistal myopathy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 4
Oculopharyngodistal myopathy Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 4
Oculopharyngodistal myopathy Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 4
Oculopharyngodistal myopathy Finding site Upper eyelid structure true Inferred relationship Existential restriction modifier 2
Oculopharyngodistal myopathy Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Oculopharyngodistal myopathy Associated morphology Congenital prolapse false Inferred relationship Existential restriction modifier 2
Oculopharyngodistal myopathy Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Oculopharyngodistal myopathy Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Oculopharyngodistal myopathy Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 1
Oculopharyngodistal myopathy Finding site Muscle structure of pharynx false Inferred relationship Existential restriction modifier 3
Oculopharyngodistal myopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Oculopharyngodistal myopathy Clinical course Progressive true Inferred relationship Existential restriction modifier 1
Oculopharyngodistal myopathy Is a Ptosis of eyelid true Inferred relationship Existential restriction modifier
Oculopharyngodistal myopathy Finding site Muscle structure of pharynx true Inferred relationship Existential restriction modifier 3
Oculopharyngodistal myopathy Is a Chronic disease of respiratory system true Inferred relationship Existential restriction modifier
Oculopharyngodistal myopathy Is a Chronic digestive system disorder true Inferred relationship Existential restriction modifier
Oculopharyngodistal myopathy Is a Chronic disease of ocular adnexa true Inferred relationship Existential restriction modifier
Oculopharyngodistal myopathy Is a Chronic disease of musculoskeletal system false Inferred relationship Existential restriction modifier
Oculopharyngodistal myopathy Associated morphology Prolapse true Inferred relationship Existential restriction modifier 2
Oculopharyngodistal myopathy Is a Musculoskeletal disorder of the neck true Inferred relationship Existential restriction modifier
Oculopharyngodistal myopathy Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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