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771342004: Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3705834019 Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3705835018 Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3705836017 MRCS syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3705837014 MRCS (microcornea, rod-cone dystrophy, cataract, posterior staphyloma) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3705838016 A rare genetic retinal dystrophy disorder with characteristics of bilateral microcornea, rod-cone dystrophy, cataracts and posterior staphyloma, in the absence of other systemic features. Night blindness is typically the presenting manifestation and nystagmus, strabismus, astigmatism and angle closure glaucoma may be associated findings. Progressive visual acuity deterioration, due to pulverulent-like cataracts, results in poor vision ranging from no light perception to 20/400. There is evidence the disease is caused by heterozygous mutation in the bestrophin-1 gene (BEST1) on chromosome 11q12. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3705834019 Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3705835018 Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3705836017 MRCS syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3705837014 MRCS (microcornea, rod-cone dystrophy, cataract, posterior staphyloma) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3705838016 A rare genetic retinal dystrophy disorder with characteristics of bilateral microcornea, rod-cone dystrophy, cataracts and posterior staphyloma, in the absence of other systemic features. Night blindness is typically the presenting manifestation and nystagmus, strabismus, astigmatism and angle closure glaucoma may be associated findings. Progressive visual acuity deterioration, due to pulverulent-like cataracts, results in poor vision ranging from no light perception to 20/400. There is evidence the disease is caused by heterozygous mutation in the bestrophin-1 gene (BEST1) on chromosome 11q12. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
574931000274114 Syndrom mit Mikrokornea, Zapfen-Stäbchen-Dystrophie, Katarakt und posteriorem Staphylom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3408061001000114 MRCS-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
574931000274114 Syndrom mit Mikrokornea, Zapfen-Stäbchen-Dystrophie, Katarakt und posteriorem Staphylom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3408061001000114 MRCS-Syndrom 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
Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder) Associated morphology Cataract false Inferred relationship Existential restriction modifier (core metadata concept) 2
Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder) Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder) Finding site Structure of lens of eye (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder) Is a Cataract true Inferred relationship Existential restriction modifier (core metadata concept)
Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder) Is a Hereditary retinal dystrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder) Associated morphology Opacity true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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