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232054005: X-linked retinitis pigmentosa (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
347705019 X-linked retinitis pigmentosa en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
620069017 X-linked retinitis pigmentosa (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) 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 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
X-linked retinitis pigmentosa Is a X-linked hereditary disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Chromosome Xp11.3 microdeletion syndrome (disorder) 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 (disorder) Is a True X-linked retinitis pigmentosa Inferred relationship Some

Reference Sets

GB English

US English

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