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232052009: Autosomal dominant retinitis pigmentosa (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
347703014 Autosomal dominant retinitis pigmentosa en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
620067015 Autosomal dominant retinitis pigmentosa (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
347703014 Autosomal dominant retinitis pigmentosa en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
347703014 Autosomal dominant retinitis pigmentosa en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
620067015 Autosomal dominant retinitis pigmentosa (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
620067015 Autosomal dominant retinitis pigmentosa (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
543781000274113 Autosomal-dominante Retinitis pigmentosa de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5781901000241112 rétinite pigmentaire autosomique dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5781901000241112 rétinite pigmentaire autosomique dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
543781000274113 Autosomal-dominante Retinitis pigmentosa de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Kleinwuchs, osteochondrodysplastischer - Schwerhörigkeit - Retinitis pigmentosa Is a False Autosomal dominant retinitis pigmentosa Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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