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722990003: Congenital atrophy of optic nerve (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3334096018 Congenital atrophy of optic nerve (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3334097010 Congenital atrophy of optic nerve en Synonym Active Entire term case insensitive SNOMED CT core module
3334098017 Congenital optic atrophy en Synonym Active Entire term case insensitive SNOMED CT core module

8 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital atrophy of optic nerve Is a Congenital disease true Inferred relationship Existential restriction modifier
Congenital atrophy of optic nerve Is a Optic atrophy true Inferred relationship Existential restriction modifier
Congenital atrophy of optic nerve Associated morphology Atrophy true Inferred relationship Existential restriction modifier 1
Congenital atrophy of optic nerve Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital atrophy of optic nerve Finding site Optic nerve structure true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Leber plus disease Is a True Congenital atrophy of optic nerve Inferred relationship Existential restriction modifier
Early-onset X-linked optic atrophy Is a True Congenital atrophy of optic nerve Inferred relationship Existential restriction modifier
Severe X-linked intellectual disability Gustavson type Is a True Congenital atrophy of optic nerve Inferred relationship Existential restriction modifier
Spastic paraplegia, optic atrophy, neuropathy syndrome Is a False Congenital atrophy of optic nerve Inferred relationship Existential restriction modifier
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome Is a True Congenital atrophy of optic nerve Inferred relationship Existential restriction modifier
Wolfram-like syndrome Is a True Congenital atrophy of optic nerve Inferred relationship Existential restriction modifier
Combined immunodeficiency with faciooculoskeletal anomalies syndrome Is a True Congenital atrophy of optic nerve Inferred relationship Existential restriction modifier
Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder Is a False Congenital atrophy of optic nerve Inferred relationship Existential restriction modifier
Optic atrophy due to late congenital syphilis Is a True Congenital atrophy of optic nerve Inferred relationship Existential restriction modifier
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Is a True Congenital atrophy of optic nerve Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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