FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

232055006: X-linked retinitis pigmentosa heterozygote (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
347706018 X-linked retinitis pigmentosa heterozygote en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
620070016 X-linked retinitis pigmentosa heterozygote (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
347706018 X-linked retinitis pigmentosa heterozygote en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
620070016 X-linked retinitis pigmentosa heterozygote (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
620070016 X-linked retinitis pigmentosa heterozygote (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
636951000274119 Heterozygote X-chromosomale Retinitis pigmentosa de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
636951000274119 Heterozygote X-chromosomale 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
X-linked retinitis pigmentosa heterozygote (disorder) Is a Retinitis pigmentosa (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
X-linked retinitis pigmentosa heterozygote (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept)
X-linked retinitis pigmentosa heterozygote (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked retinitis pigmentosa heterozygote (disorder) Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked retinitis pigmentosa heterozygote (disorder) Is a X-linked retinitis pigmentosa true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start