FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

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


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 Some
Autosomal dominant retinitis pigmentosa Finding site Retinal structure false Inferred relationship Some
Autosomal dominant retinitis pigmentosa Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant retinitis pigmentosa Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal dominant retinitis pigmentosa Finding site Retinal structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome (disorder) Is a True Autosomal dominant retinitis pigmentosa Inferred relationship Some

This concept is not in any reference sets

Back to Start