FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

400954002: Euryblepharon (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
1768875016 Euryblepharon (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1780162010 Euryblepharon en Synonym Active Entire term case insensitive SNOMED CT core module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Euryblepharon Is a Congenital anomaly of eyelid true Inferred relationship Existential restriction modifier
Euryblepharon Finding site Structure of orbit proper false Inferred relationship Existential restriction modifier 2
Euryblepharon Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Euryblepharon Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Euryblepharon Occurrence Congenital false Inferred relationship Existential restriction modifier
Euryblepharon Finding site Eyelid structure false Inferred relationship Existential restriction modifier 1
Euryblepharon Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Euryblepharon Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Euryblepharon Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Euryblepharon Finding site Eyelid structure true Inferred relationship Existential restriction modifier 1
Euryblepharon Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Euryblepharon Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Euryblepharon Finding site Eyelid structure false Inferred relationship Existential restriction modifier 2
Euryblepharon Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Euryblepharon Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Euryblepharon Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Euryblepharon of bilateral eyelids Is a True Euryblepharon Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start