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765191009: Kandori fleck retina syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3657394016 Kandori fleck retina syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3657395015 Kandori fleck retina syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3657396019 Fleck retina of Kandori en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5404503014 Kandori fleck retina is a rare, genetic retinal dystrophy disorder characterized by irregular, sharply defined, yellowish-white lesions of variable size that are distributed mainly in the nasal equatorial region of the retina, with a tendency to confluence, that are not associated with any vascular or optic nerve abnormalities. They frequently manifest as mild and stationary night blindness. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404504015 Kandori fleck retina is a rare, genetic retinal dystrophy disorder characterised by irregular, sharply defined, yellowish-white lesions of variable size that are distributed mainly in the nasal equatorial region of the retina, with a tendency to confluence, that are not associated with any vascular or optic nerve abnormalities. They frequently manifest as mild and stationary night blindness. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3657394016 Kandori fleck retina syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3657395015 Kandori fleck retina syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3657396019 Fleck retina of Kandori en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3657393010 A rare genetic retinal dystrophy with characteristics of irregular, sharply defined, yellowish-white lesions of variable size that are distributed mainly in the nasal equatorial region of the retina, with a tendency to confluence, that are not associated with any vascular or optic nerve abnormalities. They frequently manifest as mild and stationary night blindness. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404503014 Kandori fleck retina is a rare, genetic retinal dystrophy disorder characterized by irregular, sharply defined, yellowish-white lesions of variable size that are distributed mainly in the nasal equatorial region of the retina, with a tendency to confluence, that are not associated with any vascular or optic nerve abnormalities. They frequently manifest as mild and stationary night blindness. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404504015 Kandori fleck retina is a rare, genetic retinal dystrophy disorder characterised by irregular, sharply defined, yellowish-white lesions of variable size that are distributed mainly in the nasal equatorial region of the retina, with a tendency to confluence, that are not associated with any vascular or optic nerve abnormalities. They frequently manifest as mild and stationary night blindness. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
543041000274118 Gefleckte Netzhaut nach Kandori de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3391891001000113 Gefleckte Retina nach Kandori de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6347281000241110 syndrome de la rétine mouchetée de Kandori fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6347291000241112 syndrome de Kandori fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6347281000241110 syndrome de la rétine mouchetée de Kandori fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6347291000241112 syndrome de Kandori fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
543041000274118 Gefleckte Netzhaut nach Kandori de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3391891001000113 Gefleckte Retina nach Kandori 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
Kandori fleck retina syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Kandori fleck retina syndrome (disorder) Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Kandori fleck retina syndrome (disorder) Is a Hereditary retinal dystrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Kandori fleck retina syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Kandori fleck retina syndrome (disorder) Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)
Kandori fleck retina syndrome (disorder) Associated morphology Dystrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Kandori fleck retina syndrome (disorder) Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Kandori fleck retina syndrome (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 2
Kandori fleck retina syndrome (disorder) Is a Retinal flecking (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Kandori fleck retina syndrome (disorder) Associated morphology Deposition true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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