FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

1187543005: Dystrophy of retina due to GM2 gangliosidosis (disorder)


Status: current, Defined. Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4674116014 Retinal dystrophy due to GM2 gangliosidosis en Synonym Active Initial character case insensitive SNOMED CT core
4674524010 Dystrophy of retina due to GM2 gangliosidosis en Synonym Active Initial character case insensitive SNOMED CT core
4674525011 Dystrophy of retina due to GM2 gangliosidosis (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinal dystrophy due to GM2 gangliosidosis Is a Retinal dystrophy true Inferred relationship Some
Retinal dystrophy due to GM2 gangliosidosis Due to GM2 gangliosidosis true Inferred relationship Some 2
Retinal dystrophy due to GM2 gangliosidosis Finding site Retinal structure true Inferred relationship Some 1
Retinal dystrophy due to GM2 gangliosidosis Associated morphology Dystrophy true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Back to Start