659321000000103: Hereditary optic atrophy NOS (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 01-Apr 2012. Module: SNOMED CT United Kingdom clinical extension module

Descriptions:

Id Description Lang Type Status Case? Module

1448411000000113 Hereditary optic atrophy NOS (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module

1448421000000119 Hereditary optic atrophy NOS en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary optic atrophy NOS	Is a	Hereditary optic atrophy	false	Inferred relationship	Existential restriction modifier
Hereditary optic atrophy NOS	Associated morphology	Primary atrophy	false	Inferred relationship	Existential restriction modifier	1
Hereditary optic atrophy NOS	Finding site	Optic nerve structure	false	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets