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95486002: Congenital blindness (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
158165015 Congenital blindness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
839649014 Congenital blindness (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
158165015 Congenital blindness en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
158165015 Congenital blindness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
839649014 Congenital blindness (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
839649014 Congenital blindness (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
392381000274110 Angeborene Blindheit de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
627021000274112 Kongenitale Blindheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
317851000172116 cécité congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
317851000172116 cécité congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
392381000274110 Angeborene Blindheit de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
627021000274112 Kongenitale Blindheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital blindness Is a Congenital anomaly of eye false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital blindness Is a Vision problem false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital blindness Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blindness Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital blindness Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital blindness Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital blindness Finding site Orbital region structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blindness Is a Congenital anomaly of visual system true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital blindness Finding site The eye, ocular adnexa, afferent visual pathways, efferent visual pathways, and pupil innervation pathways true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blindness Is a Blindness AND/OR vision impairment level true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital blindness Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blindness Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blindness Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital blindness Interprets Vision observable (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital blindness Has interpretation Impaired (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blindness Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital blindness Interprets Vision, function (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital blindness Interprets Visual function (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital blindness Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital blindness Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blindness Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital blindness Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blindness Interprets Visual function (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital blindness Interprets Visual function (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital blindness Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital blindness Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blindness Interprets Visual function (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blindness Interprets Visual function (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital blindness Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blindness Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital blindness Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital blindness Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital blindness Finding site The eye, ocular adnexa, afferent visual pathways, efferent visual pathways, and pupil innervation pathways false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital blindness Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blindness Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blindness Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Microphthalmia with brain atrophy syndrome (disorder) Is a True Congenital blindness Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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