1192004: Familial amyloid neuropathy, Finnish type (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module

3120012 Familial amyloid neuropathy, Finnish type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

705455016 Familial amyloid neuropathy, Finnish type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3120012 Familial amyloid neuropathy, Finnish type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

705455016 Familial amyloid neuropathy, Finnish type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial amyloid neuropathy, Finnish type	Is a	Familial amyloid polyneuropathy (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid neuropathy, Finnish type	Finding site	Nerve structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid neuropathy, Finnish type	Associated morphology	Amyloid deposition	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial amyloid neuropathy, Finnish type	Finding site	Peripheral nervous system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial amyloid neuropathy, Finnish type	Associated morphology	Amyloid deposition	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial amyloid neuropathy, Finnish type	Finding site	Peripheral nervous system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial amyloid neuropathy, Finnish type	Finding site	Peripheral nerve structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Lattice corneal dystrophy	Is a	False	Familial amyloid neuropathy, Finnish type	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

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

REPLACED BY association reference set (foundation metadata concept)