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230530003: Congenital nuclear ophthalmoplegia (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
345436010 Congenital nuclear ophthalmoplegia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
618350017 Congenital nuclear ophthalmoplegia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
345436010 Congenital nuclear ophthalmoplegia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
345436010 Congenital nuclear ophthalmoplegia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
618350017 Congenital nuclear ophthalmoplegia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
618350017 Congenital nuclear ophthalmoplegia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
572541000274118 Kongenitale nukleäre Ophthalmoplegie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
634491000274111 Kongenitale nukleäre Augenmuskellähmung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5822571000241110 ophtalmoplégie nucléaire congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5822571000241110 ophtalmoplégie nucléaire congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
572541000274118 Kongenitale nukleäre Ophthalmoplegie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
634491000274111 Kongenitale nukleäre Augenmuskellähmung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital nuclear ophthalmoplegia Is a Congenital disorders of eye and eyelid movements false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nuclear ophthalmoplegia Is a Ophthalmoplegia true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nuclear ophthalmoplegia Is a Disorder of brain stem (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nuclear ophthalmoplegia Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nuclear ophthalmoplegia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nuclear ophthalmoplegia Finding site Brainstem structure false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nuclear ophthalmoplegia Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nuclear ophthalmoplegia Finding site Orbital region structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nuclear ophthalmoplegia Finding site Eyelid structure false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nuclear ophthalmoplegia Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nuclear ophthalmoplegia Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nuclear ophthalmoplegia Interprets Ocular motility observable (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nuclear ophthalmoplegia Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nuclear ophthalmoplegia Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nuclear ophthalmoplegia Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nuclear ophthalmoplegia Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nuclear ophthalmoplegia Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nuclear ophthalmoplegia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital nuclear ophthalmoplegia Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nuclear ophthalmoplegia Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nuclear ophthalmoplegia Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nuclear ophthalmoplegia Finding site Medial longitudinal fasciculus structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nuclear ophthalmoplegia Is a Disorder of midbrain (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nuclear ophthalmoplegia Finding site Eyelid structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital nuclear ophthalmoplegia Finding site Medial longitudinal fasciculus structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nuclear ophthalmoplegia Finding site Eyelid structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nuclear ophthalmoplegia Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nuclear ophthalmoplegia Is a Congenital anomaly of eyelid true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nuclear ophthalmoplegia Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nuclear ophthalmoplegia Is a Dysgenesis of the brainstem true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nuclear ophthalmoplegia Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital nuclear ophthalmoplegia Interprets Movement observable true Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital nuclear ophthalmoplegia Has interpretation Absent true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome (disorder) Is a True Congenital nuclear ophthalmoplegia Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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