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230530003: Congenital nuclear ophthalmoplegia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
345436010 Congenital nuclear ophthalmoplegia en Synonym Active Entire term case insensitive SNOMED CT core module
618350017 Congenital nuclear ophthalmoplegia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core 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
Congenital nuclear ophthalmoplegia Is a Ophthalmoplegia true Inferred relationship Existential restriction modifier
Congenital nuclear ophthalmoplegia Is a Disorder of brain stem false Inferred relationship Existential restriction modifier
Congenital nuclear ophthalmoplegia Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital nuclear ophthalmoplegia Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital nuclear ophthalmoplegia Finding site Brainstem structure false Inferred relationship Existential restriction modifier
Congenital nuclear ophthalmoplegia Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 1
Congenital nuclear ophthalmoplegia Finding site Orbital region structure false Inferred relationship Existential restriction modifier 1
Congenital nuclear ophthalmoplegia Finding site Eyelid structure false Inferred relationship Existential restriction modifier
Congenital nuclear ophthalmoplegia Has interpretation Abnormal false Inferred relationship Existential restriction modifier
Congenital nuclear ophthalmoplegia Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital nuclear ophthalmoplegia Interprets Ocular motility observable false Inferred relationship Existential restriction modifier
Congenital nuclear ophthalmoplegia Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital nuclear ophthalmoplegia Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 1
Congenital nuclear ophthalmoplegia Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital nuclear ophthalmoplegia Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Congenital nuclear ophthalmoplegia Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 2
Congenital nuclear ophthalmoplegia Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Congenital nuclear ophthalmoplegia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital nuclear ophthalmoplegia Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital nuclear ophthalmoplegia Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Congenital nuclear ophthalmoplegia Finding site Medial longitudinal fasciculus structure false Inferred relationship Existential restriction modifier 2
Congenital nuclear ophthalmoplegia Is a Disorder of midbrain true Inferred relationship Existential restriction modifier
Congenital nuclear ophthalmoplegia Finding site Eyelid structure false Inferred relationship Existential restriction modifier 3
Congenital nuclear ophthalmoplegia Finding site Medial longitudinal fasciculus structure true Inferred relationship Existential restriction modifier 1
Congenital nuclear ophthalmoplegia Finding site Eyelid structure true Inferred relationship Existential restriction modifier 2
Congenital nuclear ophthalmoplegia Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Congenital nuclear ophthalmoplegia Is a Congenital anomaly of eyelid true Inferred relationship Existential restriction modifier
Congenital nuclear ophthalmoplegia Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Congenital nuclear ophthalmoplegia Is a Dysgenesis of the brainstem true Inferred relationship Existential restriction modifier
Congenital nuclear ophthalmoplegia Interprets Movement true Inferred relationship Existential restriction modifier 4
Congenital nuclear ophthalmoplegia Interprets Movement observable true Inferred relationship Existential restriction modifier 3
Congenital nuclear ophthalmoplegia Has interpretation Absent true Inferred relationship Existential restriction modifier 3

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

This concept is not in any reference sets

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