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232058008: Usher syndrome type 2 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
347709013 Usher syndrome type 2 en Synonym Active Case sensitive SNOMED CT core
620074013 Usher syndrome type 2 (disorder) en Fully specified name Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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