FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

232054005: X-linked retinitis pigmentosa (disorder)


Status: current, Defined. Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
347705019 X-linked retinitis pigmentosa en Synonym Active Case sensitive SNOMED CT core
620069017 X-linked retinitis pigmentosa (disorder) en Fully specified name Active Case sensitive SNOMED CT core


3 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Chromosome Xp11.3 microdeletion syndrome Is a True X-linked retinitis pigmentosa Inferred relationship Some
X-linked retinitis pigmentosa heterozygote Is a True X-linked retinitis pigmentosa Inferred relationship Some
Primary ciliary dyskinesia and retinitis pigmentosa syndrome Is a True X-linked retinitis pigmentosa Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Back to Start