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770626007: Congenital Horner syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3701687013 Congenital Horner syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3701688015 Congenital Horner syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
3701689011 Congenital Claude Bernard Horner syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital Horner syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital Horner syndrome Is a Horner's syndrome pupil true Inferred relationship Existential restriction modifier
Congenital Horner syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Congenital Horner syndrome Is a Inherited autonomic nervous system disorder true Inferred relationship Existential restriction modifier
Congenital Horner syndrome Is a Congenital ptosis true Inferred relationship Existential restriction modifier
Congenital Horner syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Congenital Horner syndrome Interprets Pupil constriction true Inferred relationship Existential restriction modifier 4
Congenital Horner syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital Horner syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Congenital Horner syndrome Finding site Upper eyelid structure true Inferred relationship Existential restriction modifier 1
Congenital Horner syndrome Finding site Pupil structure true Inferred relationship Existential restriction modifier 3
Congenital Horner syndrome Finding site Autonomic nerve structure true Inferred relationship Existential restriction modifier 2
Congenital Horner syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital Horner syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Congenital Horner syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Congenital Horner syndrome Associated morphology Prolapse true Inferred relationship Existential restriction modifier 1
Congenital Horner syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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