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

1263461006: Isolated congenital distichiasis (disorder)


Status: current, Primitive. Date: 31-Jan 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5168752011 Isolated congenital distichiasis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
5168753018 Isolated distichiasis en Synonym Active Case insensitive SNOMED CT core
5168755013 Isolated congenital distichiasis en Synonym Active Case insensitive SNOMED CT core
5168754012 Isolated distichiasis is a rare congenital eyelid anomaly. The disease has characteristics of an accessory row of eyelashes (that may be partial or complete) posterior to the normal row of cilia, at or close to the meibomian gland orifices. This is not associated with any other condition and that may lead to ocular irritation and corneal damage if left untreated. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Isolated distichiasis Occurrence Congenital true Inferred relationship Some 1
Isolated distichiasis Finding site Structure of eyelash true Inferred relationship Some 1
Isolated distichiasis Pathological process Pathological developmental process true Inferred relationship Some 1
Isolated distichiasis Occurrence Congenital true Inferred relationship Some 2
Isolated distichiasis Finding site Structure of eyelash true Inferred relationship Some 2
Isolated distichiasis Associated morphology Double structure true Inferred relationship Some 2
Isolated distichiasis Pathological process Pathological developmental process true Inferred relationship Some 2
Isolated distichiasis Is a Congenital distichiasis true Inferred relationship Some
Isolated distichiasis Associated morphology Congenital ectopia true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start