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719282008: Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3315827019 Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315828012 Primary ciliary dyskinesia and retinitis pigmentosa syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315829016 An X-linked ciliary dysfunction disorder of both the respiratory epithelium and photoreceptors of the retina. This leads to ocular problems including mild night blindness, constriction of the visual field and scotopic and photopic ERG responses reduced to 30-60%. It is also associated with primary ciliary dyskinesia manifestations including chronic bronchorrhea with bronchoectasis and chronic sinusitis along with sensorineural hearing loss. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3315830014 An X-linked ciliary dysfunction disorder of both the respiratory epithelium and photoreceptors of the retina. This leads to ocular problems including mild night blindness, constriction of the visual field and scotopic and photopic ERG responses reduced to 30-60%. It is also associated with primary ciliary dyskinesia manifestations including chronic bronchorrhoea with bronchoectasis and chronic sinusitis along with sensorineural hearing loss. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
930151000172113 syndrome de dyskinésie ciliaire primitive-rétinite pigmentaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
1756621000172119 syndrome de dyskinésie ciliaire primitive avec rétinite pigmentaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
1014231000172116 primaire ciliaire dyskinesie, retinitis pigmentosa-syndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Is a Retinitis pigmentosa false Inferred relationship Some
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Is a Immotile cilia syndrome false Inferred relationship Some
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Is a X-linked hereditary disease false Inferred relationship Some
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Occurrence Congenital false Inferred relationship Some 2
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Associated morphology Dystrophy true Inferred relationship Some 3
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Finding site Retinal structure true Inferred relationship Some 3
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Associated morphology Dystrophy false Inferred relationship Some 2
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Finding site Retinal structure false Inferred relationship Some 2
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 3
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Occurrence Congenital false Inferred relationship Some 3
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Associated morphology defect false Inferred relationship Some 1
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Finding site Respiratory tract structure false Inferred relationship Some 1
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Has interpretation Impaired true Inferred relationship Some 4
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Interprets Mucociliary clearance true Inferred relationship Some 4
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Is a Inherited mucociliary clearance defect true Inferred relationship Some
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Is a Developmental disorder false Inferred relationship Some
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Is a X-linked recessive hereditary disease true Inferred relationship Some
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Is a X-linked retinitis pigmentosa true Inferred relationship Some
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Finding site Respiratory tract structure true Inferred relationship Some 2
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Associated morphology defect false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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