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57838006: Retinitis pigmentosa-deafness syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1231772018 Usher syndrome en Synonym Active Case sensitive SNOMED CT core
796504017 Retinitis pigmentosa-deafness syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
96172019 Retinitis pigmentosa-deafness syndrome en Synonym Active Case insensitive SNOMED CT core
96173012 Usher's syndrome en Synonym Active Case sensitive SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


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

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

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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