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698848005: Hereditary retinal dystrophy primarily involving sensory retina (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2981458015 Hereditary retinal dystrophy primarily involving sensory retina en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2981465011 Inherited retinal dystrophy primarily involving sensory retina en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2981483015 Hereditary retinal dystrophy primarily involving sensory retina (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2981458015 Hereditary retinal dystrophy primarily involving sensory retina en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2981458015 Hereditary retinal dystrophy primarily involving sensory retina en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2981465011 Inherited retinal dystrophy primarily involving sensory retina en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2981465011 Inherited retinal dystrophy primarily involving sensory retina en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2981483015 Hereditary retinal dystrophy primarily involving sensory retina (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2981483015 Hereditary retinal dystrophy primarily involving sensory retina (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
515571000274110 Erbbedingte Netzhautdystrophie, sensorische Netzhaut primär betroffen de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
599761000274112 Hereditäre Retinadystrophie, sensorische Retina primär betroffen de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6265381000241110 dystrophie héréditaire de la rétine impliquant principalement la rétine sensitive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6265391000241112 dystrophie rétinienne héréditaire impliquant principalement la rétine sensorielle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6265381000241110 dystrophie héréditaire de la rétine impliquant principalement la rétine sensitive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6265391000241112 dystrophie rétinienne héréditaire impliquant principalement la rétine sensorielle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
515571000274110 Erbbedingte Netzhautdystrophie, sensorische Netzhaut primär betroffen de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
599761000274112 Hereditäre Retinadystrophie, sensorische Retina primär betroffen 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
Hereditary retinal dystrophy primarily involving sensory retina Is a Hereditary retinal dystrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary retinal dystrophy primarily involving sensory retina Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary retinal dystrophy primarily involving sensory retina Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary retinal dystrophy primarily involving sensory retina Finding site Retinal structure 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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