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253228006: Embryotoxon (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of head region\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Congenital anomaly of eye\Congenital anomaly of anterior segment of eye (disorder)\Congenital structural abnormality of cornea\Embryotoxon
\Head finding (finding)\Finding of head region\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of anterior segment of eye (disorder)\Congenital anomaly of anterior segment of eye (disorder)\Congenital structural abnormality of cornea\Embryotoxon
\Head finding (finding)\Finding of head region\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of anterior segment of eye (disorder)\Disease of cornea (disorder)\Congenital structural abnormality of cornea\Embryotoxon
\Head finding (finding)\Finding of head region\Globe finding (finding)\Anterior segment finding (finding)\Corneal finding\Disease of cornea (disorder)\Congenital structural abnormality of cornea\Embryotoxon
\Head finding (finding)\Finding of head region\Globe finding (finding)\Anterior segment finding (finding)\Disorder of anterior segment of eye (disorder)\Congenital anomaly of anterior segment of eye (disorder)\Congenital structural abnormality of cornea\Embryotoxon
\Head finding (finding)\Finding of head region\Globe finding (finding)\Anterior segment finding (finding)\Disorder of anterior segment of eye (disorder)\Disease of cornea (disorder)\Congenital structural abnormality of cornea\Embryotoxon
\Head finding (finding)\Finding of head region\Globe finding (finding)\Disorder of eye proper (disorder)\Anomaly of eye\Congenital anomaly of eye\Congenital anomaly of anterior segment of eye (disorder)\Congenital structural abnormality of cornea\Embryotoxon
\Head finding (finding)\Finding of head region\Globe finding (finding)\Disorder of eye proper (disorder)\Disorder of anterior segment of eye (disorder)\Congenital anomaly of anterior segment of eye (disorder)\Congenital structural abnormality of cornea\Embryotoxon
\Head finding (finding)\Finding of head region\Globe finding (finding)\Disorder of eye proper (disorder)\Disorder of anterior segment of eye (disorder)\Disease of cornea (disorder)\Congenital structural abnormality of cornea\Embryotoxon
\Head finding (finding)\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Congenital anomaly of eye\Congenital anomaly of anterior segment of eye (disorder)\Congenital structural abnormality of cornea\Embryotoxon
\Head finding (finding)\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of anterior segment of eye (disorder)\Congenital anomaly of anterior segment of eye (disorder)\Congenital structural abnormality of cornea\Embryotoxon
\Head finding (finding)\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of anterior segment of eye (disorder)\Disease of cornea (disorder)\Congenital structural abnormality of cornea\Embryotoxon
\Head finding (finding)\Disorder of head (disorder)\Congenital anomaly of head\Congenital anomaly of eye\Congenital anomaly of anterior segment of eye (disorder)\Congenital structural abnormality of cornea\Embryotoxon

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Embryotoxon	Is a	Congenital structural abnormality of cornea	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Embryotoxon	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Embryotoxon	Finding site	Corneal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Embryotoxon	Finding site	Nervous system structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Embryotoxon	Finding site	Orbital region structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Embryotoxon	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Embryotoxon	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Embryotoxon	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Embryotoxon	Finding site	Corneal structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Embryotoxon	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Embryotoxon	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Embryotoxon	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Embryotoxon	Finding site	Corneal structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Embryotoxon	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Embryotoxon	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Embryotoxon	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Anterior embryotoxon	Is a	False	Embryotoxon	Inferred relationship	Existential restriction modifier (core metadata concept)
Axenfeld's anomaly	Is a	False	Embryotoxon	Inferred relationship	Existential restriction modifier (core metadata concept)
Posterior embryotoxon	Is a	True	Embryotoxon	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
377130019	Embryotoxon	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
643961010	Embryotoxon (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
377130019	Embryotoxon	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
377130019	Embryotoxon	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
643961010	Embryotoxon (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
643961010	Embryotoxon (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5069991000241119	embryotoxon	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5069991000241119	embryotoxon	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module