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721200000: Early-onset X-linked optic atrophy (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
3324593011 Early-onset X-linked optic atrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3324594017 Early-onset X-linked optic atrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3324595016 Non-Leber type optic atrophy with early-onset en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3324611017 Optic atrophy type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5402632016 Early-onset X-linked optic atrophy is a rare form of hereditary optic atrophy, seen in only 4 families to date, with an onset in early childhood, characterized by progressive loss of visual acuity, significant optic nerve pallor and occasionally additional neurological manifestations, with females being unaffected. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402633014 Early-onset X-linked optic atrophy is a rare form of hereditary optic atrophy, seen in only 4 families to date, with an onset in early childhood, characterised by progressive loss of visual acuity, significant optic nerve pallor and occasionally additional neurological manifestations, with females being unaffected. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3324593011 Early-onset X-linked optic atrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3324594017 Early-onset X-linked optic atrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3324595016 Non-Leber type optic atrophy with early-onset en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3324611017 Optic atrophy type 2 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3324611017 Optic atrophy type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3324612012 A rare form of hereditary optic atrophy seen in only 4 families to date. With onset in early childhood the disease has characteristics of progressive loss of visual acuity, significant optic nerve pallor and occasionally additional neurological manifestations, with females being unaffected. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402632016 Early-onset X-linked optic atrophy is a rare form of hereditary optic atrophy, seen in only 4 families to date, with an onset in early childhood, characterized by progressive loss of visual acuity, significant optic nerve pallor and occasionally additional neurological manifestations, with females being unaffected. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402633014 Early-onset X-linked optic atrophy is a rare form of hereditary optic atrophy, seen in only 4 families to date, with an onset in early childhood, characterised by progressive loss of visual acuity, significant optic nerve pallor and occasionally additional neurological manifestations, with females being unaffected. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
601711000274118 OPA2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
601721000274113 X-chromosomale Optikusatrophie mit frühem Beginn de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
909101000172110 atrophie optique précoce liée à l'X fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
965281000172110 atrophie optique précoce de type non-Leber fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
909101000172110 atrophie optique précoce liée à l'X fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
965281000172110 atrophie optique précoce de type non-Leber fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
601711000274118 OPA2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
601721000274113 X-chromosomale Optikusatrophie mit frühem Beginn de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3435751001000110 Optikusatrophie, X-chromosomale, mit frühem Beginn de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Early-onset X-linked optic atrophy (disorder) Is a Hereditary optic atrophy (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Early-onset X-linked optic atrophy (disorder) Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
Early-onset X-linked optic atrophy (disorder) Associated morphology Primary atrophy true Inferred relationship Existential restriction modifier (core metadata concept) 2
Early-onset X-linked optic atrophy (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Early-onset X-linked optic atrophy (disorder) Finding site Optic nerve structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Early-onset X-linked optic atrophy (disorder) Is a Congenital atrophy of optic nerve (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Early-onset X-linked optic atrophy (disorder) Is a X-linked recessive hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
Early-onset X-linked optic atrophy (disorder) Is a X-linked optic atrophy true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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