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73119000: Retinitis pigmentosa-deafness-ataxia 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
121439016 Retinitis pigmentosa-deafness-ataxia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
121440019 Hallgren's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
813472015 Retinitis pigmentosa-deafness-ataxia syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinitis pigmentosa-deafness-ataxia syndrome Is a Retinitis pigmentosa-deafness syndrome true Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness-ataxia syndrome Finding site Retinal structure false Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness-ataxia syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Retinitis pigmentosa-deafness-ataxia syndrome Finding site Retinal structure true Inferred relationship Existential restriction modifier 1
Retinitis pigmentosa-deafness-ataxia syndrome Finding site Structure of auditory system false Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness-ataxia syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 3
Retinitis pigmentosa-deafness-ataxia syndrome Interprets Functional observable false Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness-ataxia syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Retinitis pigmentosa-deafness-ataxia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Retinitis pigmentosa-deafness-ataxia syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Retinitis pigmentosa-deafness-ataxia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Retinitis pigmentosa-deafness-ataxia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Retinitis pigmentosa-deafness-ataxia syndrome Finding site Structure of auditory system 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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