FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

1187520001: Leigh syndrome due to cytochrome C oxidase deficiency (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4674069013 Leigh syndrome due to cytochrome C oxidase deficiency (disorder) en Fully specified name Active Case sensitive SNOMED CT core
4674070014 Leigh syndrome due to cytochrome C oxidase deficiency en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Leigh syndrome due to cytochrome C oxidase deficiency Is a Leigh's disease true Inferred relationship Some
Leigh syndrome due to cytochrome C oxidase deficiency Is a Central nervous system complication true Inferred relationship Some
Leigh syndrome due to cytochrome C oxidase deficiency Due to Cytochrome-c oxidase deficiency true Inferred relationship Some 1
Leigh syndrome due to cytochrome C oxidase deficiency Finding site Brain structure true Inferred relationship Some 2
Leigh syndrome due to cytochrome C oxidase deficiency Associated morphology Degenerative abnormality true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start