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57838006: Retinitis pigmentosa-deafness 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
96172019 Retinitis pigmentosa-deafness syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
96173012 Usher's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
796504017 Retinitis pigmentosa-deafness syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1231772018 Usher syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinitis pigmentosa-deafness syndrome Is a Multisystem disorder U-V false Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness syndrome Is a Retinitis pigmentosa false Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness syndrome Finding site Retinal structure false Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness syndrome Is a Multisystem disorder false Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Retinitis pigmentosa-deafness syndrome Finding site Retinal structure true Inferred relationship Existential restriction modifier 1
Retinitis pigmentosa-deafness syndrome Is a Autosomal recessive retinitis pigmentosa true Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness syndrome Is a Congenital malformation true Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness syndrome Is a Congenital sensorineural hearing loss true Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness syndrome Finding site Structure of auditory system false Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 3
Retinitis pigmentosa-deafness syndrome Interprets Functional observable false Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Retinitis pigmentosa-deafness syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Retinitis pigmentosa-deafness syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Retinitis pigmentosa-deafness syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Retinitis pigmentosa-deafness syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Retinitis pigmentosa-deafness syndrome Finding site Structure of auditory system true Inferred relationship Existential restriction modifier 4
Retinitis pigmentosa-deafness syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Usher syndrome type 1 Is a True Retinitis pigmentosa-deafness syndrome Inferred relationship Existential restriction modifier
Usher syndrome type 2 Is a True Retinitis pigmentosa-deafness syndrome Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness-ataxia syndrome Is a True Retinitis pigmentosa-deafness syndrome Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness syndrome type 3 Is a True Retinitis pigmentosa-deafness syndrome Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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