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778042000: Foveal hypoplasia with presenile cataract syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3737478019 O'Donnell Pappas syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3737479010 Foveal hypoplasia with presenile cataract syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3737480013 Foveal hypoplasia with presenile cataract syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


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 true Inferred relationship Existential restriction modifier
Foveal hypoplasia with presenile cataract syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Foveal hypoplasia with presenile cataract syndrome Is a Congenital hypoplasia of fovea centralis true Inferred relationship Existential restriction modifier
Foveal hypoplasia with presenile cataract syndrome Associated morphology Cataract false Inferred relationship Existential restriction modifier 2
Foveal hypoplasia with presenile cataract syndrome Is a Congenital nystagmus true Inferred relationship Existential restriction modifier
Foveal hypoplasia with presenile cataract syndrome Is a Presenile cataract true Inferred relationship Existential restriction modifier
Foveal hypoplasia with presenile cataract syndrome Finding site Structure of fovea centralis true Inferred relationship Existential restriction modifier 1
Foveal hypoplasia with presenile cataract syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Foveal hypoplasia with presenile cataract syndrome Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 1
Foveal hypoplasia with presenile cataract syndrome Interprets Ocular motility observable true Inferred relationship Existential restriction modifier 3
Foveal hypoplasia with presenile cataract syndrome Finding site Structure of lens of eye true Inferred relationship Existential restriction modifier 2
Foveal hypoplasia with presenile cataract syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Foveal hypoplasia with presenile cataract syndrome Associated morphology Abnormally opaque structure true Inferred relationship Existential restriction modifier 2
Foveal hypoplasia with presenile cataract syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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