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778042000: syndroom van foveale hypoplasie en preseniel cataract (aandoening)


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
3737478019 O'Donnell Pappas syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3737479010 Foveal hypoplasia with presenile cataract syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3737480013 Foveal hypoplasia with presenile cataract syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
12576261000146115 syndroom van foveale hypoplasie en preseniel cataract (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12576271000146114 syndroom van foveale hypoplasie en preseniel cataract nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3737481012 A rare genetic ocular disease with characteristics of congenital nystagmus (horizontal, vertical and/or torsional), foveal hypoplasia, presenile cataracts (with typical onset in the second to third decade of life) and normal irides. Corneal pannus and/or optic nerve hypoplasia may also be present. Caused by heterozygous mutation in the PAX6 gene on chromosome 11p13. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Foveal hypoplasia with presenile cataract syndrome Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Some
Foveal hypoplasia with presenile cataract syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Foveal hypoplasia with presenile cataract syndrome Is a Congenital hypoplasia of fovea centralis (disorder) true Inferred relationship Some
Foveal hypoplasia with presenile cataract syndrome Associated morphology cataract false Inferred relationship Some 2
Foveal hypoplasia with presenile cataract syndrome Is a Congenital nystagmus true Inferred relationship Some
Foveal hypoplasia with presenile cataract syndrome Is a Presenile cataract true Inferred relationship Some
Foveal hypoplasia with presenile cataract syndrome Finding site Structure of fovea centralis true Inferred relationship Some 1
Foveal hypoplasia with presenile cataract syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Foveal hypoplasia with presenile cataract syndrome Associated morphology Hypoplasia true Inferred relationship Some 1
Foveal hypoplasia with presenile cataract syndrome Interprets Ocular motility observable true Inferred relationship Some 3
Foveal hypoplasia with presenile cataract syndrome Finding site Lens clear true Inferred relationship Some 2
Foveal hypoplasia with presenile cataract syndrome Occurrence Congenital true Inferred relationship Some 1
Foveal hypoplasia with presenile cataract syndrome Associated morphology Opacity true Inferred relationship Some 2
Foveal hypoplasia with presenile cataract syndrome Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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