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232052009: Autosomal dominant retinitis pigmentosa (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2002. Module: SNOMED CT core module

Descriptions:

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


1 descendants. Search Descendants:

Expanded Value Set


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

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

This concept is not in any reference sets

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