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253212001: Epiblepharon (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of head and neck region\Head finding\...

\Finding of head region\Disorder of eye region\Disorder of ocular adnexa\Congenital anomaly of ocular adnexa\Congenital anomaly of eyelid\Epiblepharon
\Finding of head region\Disorder of eye region\Disorder of ocular adnexa\Disorder of eyelid\Congenital anomaly of eyelid\Epiblepharon
\Finding of head region\Finding of face\Eyelid finding\Disorder of eyelid\Congenital anomaly of eyelid\Epiblepharon
\Finding of head region\Finding of face\Disorder of face\Congenital anomaly of face\Congenital anomaly of eyelid\Epiblepharon
\Finding of head region\Finding of face\Disorder of face\Disorder of eyelid\Congenital anomaly of eyelid\Epiblepharon

\Disorder of head\Disorder of eye region\Disorder of ocular adnexa\Congenital anomaly of ocular adnexa\Congenital anomaly of eyelid\Epiblepharon
\Disorder of head\Disorder of eye region\Disorder of ocular adnexa\Disorder of eyelid\Congenital anomaly of eyelid\Epiblepharon
\Disorder of head\Disorder of face\Congenital anomaly of face\Congenital anomaly of eyelid\Epiblepharon
\Disorder of head\Disorder of face\Disorder of eyelid\Congenital anomaly of eyelid\Epiblepharon
\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Congenital anomaly of eyelid\Epiblepharon
\Disorder of head\Congenital anomaly of head\Congenital anomaly of ocular adnexa\Congenital anomaly of eyelid\Epiblepharon

\Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of ocular adnexa\Congenital anomaly of ocular adnexa\Congenital anomaly of eyelid\Epiblepharon
\Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of ocular adnexa\Disorder of eyelid\Congenital anomaly of eyelid\Epiblepharon
\Disease\Disorder of body system\Visual system disorder\Congenital anomaly of visual system\Congenital anomaly of ocular adnexa\Congenital anomaly of eyelid\Epiblepharon
\Disease\Disorder of head\Disorder of eye region\Disorder of ocular adnexa\Congenital anomaly of ocular adnexa\Congenital anomaly of eyelid\Epiblepharon
\Disease\Disorder of head\Disorder of eye region\Disorder of ocular adnexa\Disorder of eyelid\Congenital anomaly of eyelid\Epiblepharon
\Disease\Disorder of head\Disorder of face\Congenital anomaly of face\Congenital anomaly of eyelid\Epiblepharon
\Disease\Disorder of head\Disorder of face\Disorder of eyelid\Congenital anomaly of eyelid\Epiblepharon
\Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Congenital anomaly of eyelid\Epiblepharon
\Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of ocular adnexa\Congenital anomaly of eyelid\Epiblepharon
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of visual system\Congenital anomaly of ocular adnexa\Congenital anomaly of eyelid\Epiblepharon
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of face\Congenital anomaly of eyelid\Epiblepharon
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of ocular adnexa\Congenital anomaly of eyelid\Epiblepharon
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of visual system\Congenital anomaly of ocular adnexa\Congenital anomaly of eyelid\Epiblepharon
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of face\Congenital anomaly of eyelid\Epiblepharon
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of ocular adnexa\Congenital anomaly of eyelid\Epiblepharon

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

377109011 Epiblepharon en Synonym Active Case insensitive SNOMED CT core
643944012 Epiblepharon (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Bilateral epiblepharon	Is a	True	Epiblepharon	Inferred relationship	Some
Congenital epiblepharon-inferior oblique syndrome	Is a	True	Epiblepharon	Inferred relationship	Some
Swan's syndrome II	Is a	False	Epiblepharon	Inferred relationship	Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
377109011	Epiblepharon	en	Synonym	Active	Case insensitive	SNOMED CT core
643944012	Epiblepharon (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core