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721200000: Early-onset X-linked optic atrophy (disorder)


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

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 SNOMED CT core module
3324594017 Early-onset X-linked optic atrophy en Synonym Active Only initial character case insensitive SNOMED CT core module
3324595016 Non-Leber type optic atrophy with early-onset en Synonym Active Only initial character case insensitive SNOMED CT core module
3324611017 Optic atrophy type 2 en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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