FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

1259560001: Congenital multi-minicore disease with external ophthalmoplegia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2023. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5157299018 Congenital multi-minicore disease with external ophthalmoplegia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5157300014 Congenital multi-minicore disease with external ophthalmoplegia en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital multi-minicore disease with external ophthalmoplegia Is a External ophthalmoplegia true Inferred relationship Existential restriction modifier
Congenital multi-minicore disease with external ophthalmoplegia Is a Multi-core congenital myopathy true Inferred relationship Existential restriction modifier
Congenital multi-minicore disease with external ophthalmoplegia Interprets Movement true Inferred relationship Existential restriction modifier 4
Congenital multi-minicore disease with external ophthalmoplegia Finding site Structure of extraocular muscle true Inferred relationship Existential restriction modifier 2
Congenital multi-minicore disease with external ophthalmoplegia Finding site Structure of nervous system true Inferred relationship Existential restriction modifier 5
Congenital multi-minicore disease with external ophthalmoplegia Interprets Movement observable true Inferred relationship Existential restriction modifier 3
Congenital multi-minicore disease with external ophthalmoplegia Has interpretation Absent true Inferred relationship Existential restriction modifier 3
Congenital multi-minicore disease with external ophthalmoplegia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital multi-minicore disease with external ophthalmoplegia Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Congenital multi-minicore disease with external ophthalmoplegia Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Congenital multi-minicore disease with external ophthalmoplegia Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start