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232052009: Autosomal dominant retinitis pigmentosa (disorder)


Status: current, Defined. Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
347703014 Autosomal dominant retinitis pigmentosa en Synonym Active Case insensitive SNOMED CT core
620067015 Autosomal dominant retinitis pigmentosa (disorder) en Fully specified name Active Case insensitive SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant retinitis pigmentosa Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant retinitis pigmentosa Is a Retinitis pigmentosa true Inferred relationship Some
Autosomal dominant retinitis pigmentosa Finding site Retinal structure false Inferred relationship Some
Autosomal dominant retinitis pigmentosa Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal dominant retinitis pigmentosa Finding site Retinal structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Is a True Autosomal dominant retinitis pigmentosa Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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