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47507006: Rieger syndrome (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
79197010 Rieger syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
784973019 Rieger syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
2620798016 Rieger's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
4592201011 Rieger anomaly 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
Rieger syndrome Is a Multiple system malformation syndrome false Inferred relationship Existential restriction modifier
Rieger syndrome Is a Congenital anomaly of anterior chamber of eye true Inferred relationship Existential restriction modifier
Rieger syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Rieger syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Rieger syndrome Finding site Structure of nervous system false Inferred relationship Existential restriction modifier
Rieger syndrome Finding site Anterior chamber of eye structure true Inferred relationship Existential restriction modifier 1
Rieger syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
Rieger syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
Rieger syndrome Finding site Anterior chamber of eye structure false Inferred relationship Existential restriction modifier 1
Rieger syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Rieger syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Rieger syndrome Finding site Anterior chamber of eye structure false Inferred relationship Existential restriction modifier 2
Rieger syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Rieger syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Rieger syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Rieger syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Rieger syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Rieger syndrome Is a Hereditary disorder of the visual system 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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