FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

268160006: Congenital corneal opacity (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
400780010 Congenital corneal opacity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
660866012 Congenital corneal opacity (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1843621000195117 opacità corneale congenita it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5107681000241114 opacité de la cornée congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
394451000274115 Angeborene Hornhauttrübung de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
534031000274110 Kongenitale Hornhauttrübung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
622741000274116 Kongenitale Trübung der Kornea de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


13 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital corneal opacity Is a Corneal opacity true Inferred relationship Some
Congenital corneal opacity Is a Congenital structural abnormality of cornea true Inferred relationship Some
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 1
Congenital corneal opacity Associated morphology anomalie du développement false Inferred relationship Some 1
Congenital corneal opacity Finding site Structure of nervous system (body structure) false Inferred relationship Some
Congenital corneal opacity Occurrence Congenital false Inferred relationship Some
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 1
Congenital corneal opacity Associated morphology Abnormally opaque structure (morphologic abnormality) false Inferred relationship Some 2
Congenital corneal opacity Associated morphology anomalie congénitale false Inferred relationship Some 1
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 1
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 2
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 2
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 1
Congenital corneal opacity Occurrence Congenital false Inferred relationship Some
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 1
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 2
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 1
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 2
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 1
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 2
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 1
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 2
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 1
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 2
Congenital corneal opacity Occurrence Congenital false Inferred relationship Some 3
Congenital corneal opacity Associated morphology anomalie du développement false Inferred relationship Some 3
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Some 3
Congenital corneal opacity Occurrence Congenital true Inferred relationship Some 1
Congenital corneal opacity Associated morphology Congenital opacity false Inferred relationship Some 1
Congenital corneal opacity Finding site Corneal structure true Inferred relationship Some 1
Congenital corneal opacity Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital corneal opacity Associated morphology Abnormally opaque structure (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital corneal opacity with visual deficit Is a True Congenital corneal opacity Inferred relationship Some
Congenital corneal opacity without visual deficit (disorder) Is a True Congenital corneal opacity Inferred relationship Some
Congenital corneal opacities NOS Is a False Congenital corneal opacity Inferred relationship Some
Congenital corneal keloid (disorder) Is a False Congenital corneal opacity Inferred relationship Some
Congenital sclerocornea Is a True Congenital corneal opacity Inferred relationship Some
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Is a False Congenital corneal opacity Inferred relationship Some
Congenital opacity of cornea of left eye Is a True Congenital corneal opacity Inferred relationship Some
Congenital opacity of cornea of right eye Is a True Congenital corneal opacity Inferred relationship Some
De Barsy syndrome (DBS) is characterized by facial dysmorphism (down-slanting palpebral fissures, a broad flat nasal bridge and a small mouth) with a progeroid appearance, large and late-closing fontanel, cutis laxa (CL), joint hyperlaxity, athetoid movements and hyperreflexia, pre- and postnatal growth retardation, intellectual deficit and developmental delay, and corneal clouding and cataract. Is a True Congenital corneal opacity Inferred relationship Some
Congenital corneal leucoma Is a True Congenital corneal opacity Inferred relationship Some
A rare genetic eye disease characterized by congenital cataract, microcornea, and corneal opacity, resulting in severe visual impairment or blindness. Depending on the genetic background, other developmental ocular defects may also be present. Is a True Congenital corneal opacity Inferred relationship Some

This concept is not in any reference sets

Back to Start