762414004: Microphthalmic socket (disorder)

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

\Head finding (finding)\Finding of head region\Disorder of eye region\Disorder of orbit proper (disorder)\Congenital structural abnormality of orbit proper (disorder)\Microphthalmic socket (disorder)
\Head finding (finding)\Finding of head region\Orbit finding\Disorder of orbit proper (disorder)\Congenital structural abnormality of orbit proper (disorder)\Microphthalmic socket (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of eye region\Disorder of orbit proper (disorder)\Congenital structural abnormality of orbit proper (disorder)\Microphthalmic socket (disorder)
\Head finding (finding)\Disorder of head (disorder)\Congenital anomaly of head\Congenital structural abnormality of orbit proper (disorder)\Microphthalmic socket (disorder)

\Eye / vision finding\Orbit finding\Disorder of orbit proper (disorder)\Congenital structural abnormality of orbit proper (disorder)\Microphthalmic socket (disorder)
\Eye / vision finding\Visual system disorder\Disorder of eye region\Disorder of orbit proper (disorder)\Congenital structural abnormality of orbit proper (disorder)\Microphthalmic socket (disorder)
\Eye / vision finding\Visual system disorder\Congenital anomaly of visual system\Congenital structural abnormality of orbit proper (disorder)\Microphthalmic socket (disorder)

\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of visual system\Congenital structural abnormality of orbit proper (disorder)\Microphthalmic socket (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital structural abnormality of orbit proper (disorder)\Microphthalmic socket (disorder)
\Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of orbit proper (disorder)\Congenital structural abnormality of orbit proper (disorder)\Microphthalmic socket (disorder)
\Disease\Disorder of body system\Visual system disorder\Congenital anomaly of visual system\Congenital structural abnormality of orbit proper (disorder)\Microphthalmic socket (disorder)
\Disease\Disorder of head (disorder)\Disorder of eye region\Disorder of orbit proper (disorder)\Congenital structural abnormality of orbit proper (disorder)\Microphthalmic socket (disorder)
\Disease\Disorder of head (disorder)\Congenital anomaly of head\Congenital structural abnormality of orbit proper (disorder)\Microphthalmic socket (disorder)
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of visual system\Congenital structural abnormality of orbit proper (disorder)\Microphthalmic socket (disorder)
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of head\Congenital structural abnormality of orbit proper (disorder)\Microphthalmic socket (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Microphthalmic socket (disorder)	Is a	Congenital structural abnormality of orbit proper (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Microphthalmic socket (disorder)	Associated morphology	Congenital smallness	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Microphthalmic socket (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Microphthalmic socket (disorder)	Finding site	Structure of orbit proper	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Microphthalmic socket (disorder)	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Microphthalmic socket (disorder)	Associated morphology	Abnormal smallness (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3636593011	Microphthalmic socket (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3636594017	Microphthalmic socket	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3636593011	Microphthalmic socket (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3636594017	Microphthalmic socket	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
541391000274110	Mikrophthalmische Augenhöhle	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
572011000274113	Mikrophthalmische Orbita	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
541391000274110	Mikrophthalmische Augenhöhle	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
572011000274113	Mikrophthalmische Orbita	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module