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718691008: Isolated cryptophthalmos (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3313231015 Isolated cryptophthalmos (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3313232010 Isolated cryptophthalmos en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3313233017 Isolated cryptophthalmia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401820015 A rare congenital abnormality in which the eyelids are absent and skin covers the ocular bulb, which is often microphthalmic. A few cases of complete bilateral cryptophthalmia have been described. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3313231015 Isolated cryptophthalmos (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3313231015 Isolated cryptophthalmos (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3313232010 Isolated cryptophthalmos en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3313232010 Isolated cryptophthalmos en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3313233017 Isolated cryptophthalmia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3313233017 Isolated cryptophthalmia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3313234011 A congenital abnormality in which the eyelids are absent and skin covers the ocular bulb, which is often microphthalmic. Six cases of complete bilateral cryptophthalmia have been described. Transmission is autosomal dominant. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401820015 A rare congenital abnormality in which the eyelids are absent and skin covers the ocular bulb, which is often microphthalmic. A few cases of complete bilateral cryptophthalmia have been described. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
563331000274119 Isolierter Kryptophthalmus de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
601351000274118 Isolierte Kryptophthalmie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6396581000241118 cryptophtalmie isolée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6396581000241118 cryptophtalmie isolée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
563331000274119 Isolierter Kryptophthalmus de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
601351000274118 Isolierte Kryptophthalmie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3452261001000110 Kryptophthalmie, isolierte de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Isolated cryptophthalmos (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Isolated cryptophthalmos (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Isolated cryptophthalmos (disorder) Is a Cryptophthalmos (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Isolated cryptophthalmos (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Isolated cryptophthalmos (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Isolated cryptophthalmos (disorder) Finding site Eyelid structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Isolated cryptophthalmos (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Isolated cryptophthalmos (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Isolated cryptophthalmos (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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