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1010610007: Retinitis pigmentosa-deafness syndrome type 3 (disorder)


Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4213324014 Usher syndrome type 3 en Synonym Active Case sensitive SNOMED CT core
4279326016 Retinitis pigmentosa-deafness syndrome type 3 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4279327013 Retinitis pigmentosa-deafness syndrome type 3 en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinitis pigmentosa-deafness syndrome type 3 Is a Retinitis pigmentosa-deafness syndrome true Inferred relationship Some
Retinitis pigmentosa-deafness syndrome type 3 Finding site Structure of auditory system true Inferred relationship Some 1
Retinitis pigmentosa-deafness syndrome type 3 Occurrence Congenital true Inferred relationship Some 1
Retinitis pigmentosa-deafness syndrome type 3 Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Retinitis pigmentosa-deafness syndrome type 3 Occurrence Congenital true Inferred relationship Some 2
Retinitis pigmentosa-deafness syndrome type 3 Pathological process Pathological developmental process true Inferred relationship Some 2
Retinitis pigmentosa-deafness syndrome type 3 Interprets Hearing true Inferred relationship Some 3
Retinitis pigmentosa-deafness syndrome type 3 Finding site Retinal structure true Inferred relationship Some 4
Retinitis pigmentosa-deafness syndrome type 3 Associated morphology Dystrophy true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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