10786008: Spinobulbar atrophy (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

18735015 Spinobulbar atrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

595265010 Spinobulbar atrophy (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

18735015 Spinobulbar atrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

595265010 Spinobulbar atrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

595265010 Spinobulbar atrophy (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Spinobulbar atrophy	Is a	Spinal cord disorder (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Spinobulbar atrophy	Is a	Congenital anomaly of nervous system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Spinobulbar atrophy	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Spinobulbar atrophy	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Spinobulbar atrophy	Finding site	Spinal cord structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Spinobulbar atrophy	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Spinobulbar atrophy	Finding site	Nervous system structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Spinobulbar atrophy	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Spinobulbar atrophy	Finding site	Nervous system structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Spinobulbar atrophy	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Spinobulbar atrophy	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Spinobulbar atrophy	Finding site	Nervous system structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

POSSIBLY EQUIVALENT TO association reference set