FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

95502000: Congenital anomaly of optic nerve (disorder)


Status: current, 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
158184017 Congenital anomaly of optic nerve en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
839670015 Congenital anomaly of optic nerve (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
158184017 Congenital anomaly of optic nerve en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
158184017 Congenital anomaly of optic nerve en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
839670015 Congenital anomaly of optic nerve (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
839670015 Congenital anomaly of optic nerve (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
627251000274112 Kongenitale Anomalie des Nervus opticus de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
627261000274110 Kongenitale Anomalie des Sehnervs de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4730951000241119 anomalie congénitale du nerf optique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4730951000241119 anomalie congénitale du nerf optique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
627251000274112 Kongenitale Anomalie des Nervus opticus de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
627261000274110 Kongenitale Anomalie des Sehnervs de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


43 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital anomaly of optic nerve Is a Congenital anomaly of visual system true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of optic nerve Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of optic nerve Is a Ear, face and neck congenital anomalies (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of optic nerve Is a Congenital anomaly of central nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of optic nerve Is a Disorder of optic nerve true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of optic nerve Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of optic nerve Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of optic nerve Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of optic nerve Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of optic nerve Finding site Optic nerve structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of optic nerve Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of optic nerve Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of optic nerve Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of optic nerve Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of optic nerve Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of optic nerve Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of optic nerve Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of optic nerve Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of optic nerve Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of optic nerve Finding site Optic nerve structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of optic nerve Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of optic nerve Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of optic nerve Finding site Optic nerve structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of optic nerve Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of optic nerve Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of optic nerve Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital anomaly of optic disc Is a True Congenital anomaly of optic nerve Inferred relationship Existential restriction modifier (core metadata concept)
Hypoplasia of the optic nerve Is a True Congenital anomaly of optic nerve Inferred relationship Existential restriction modifier (core metadata concept)
Oculocerebral dysplasia syndrome Is a False Congenital anomaly of optic nerve Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia of optic nerve (disorder) Is a True Congenital anomaly of optic nerve Inferred relationship Existential restriction modifier (core metadata concept)
Severe X-linked intellectual disability Gustavson type (disorder) Is a True Congenital anomaly of optic nerve Inferred relationship Existential restriction modifier (core metadata concept)
Combined immunodeficiency with faciooculoskeletal anomalies syndrome (disorder) Is a True Congenital anomaly of optic nerve Inferred relationship Existential restriction modifier (core metadata concept)
A disorder that is characterized by the association of a non-progressive congenital ataxia, severe intellectual deficit, optic atrophy and structural anomalies of the skin vessels. It has been described in five children from a large consanguineous Lebanese family. Short stature and microcephaly were also reported. Transmission is autosomal recessive. Is a True Congenital anomaly of optic nerve Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start