60518002: Autosomal dominant epidermolysis bullosa simplex (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

100548013 Autosomal dominant epidermolysis bullosa simplex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

100549017 EBS 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

100550017 Epidermolysis bullosa simplex, Ogna type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

498765016 Epidermolysis bullosa simplex of Ogna en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

799479010 Autosomal dominant epidermolysis bullosa simplex (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Autosomal dominant epidermolysis bullosa simplex	Is a	Epidermolysis bullosa simplex	false	Inferred relationship	Some
Autosomal dominant epidermolysis bullosa simplex	Is a	Autosomal dominant hereditary disorder	false	Inferred relationship	Some
Autosomal dominant epidermolysis bullosa simplex	Associated morphology	Blister	false	Inferred relationship	Some	2
Autosomal dominant epidermolysis bullosa simplex	Associated morphology	Epidermolysis	false	Inferred relationship	Some	2
Autosomal dominant epidermolysis bullosa simplex	Associated morphology	Keratolysis	false	Inferred relationship	Some	2
Autosomal dominant epidermolysis bullosa simplex	Finding site	Skin structure	false	Inferred relationship	Some	2
Autosomal dominant epidermolysis bullosa simplex	Finding site	Connective tissue	false	Inferred relationship	Some
Autosomal dominant epidermolysis bullosa simplex	Occurrence	Congenital	false	Inferred relationship	Some
Autosomal dominant epidermolysis bullosa simplex	Finding site	Structure of musculoskeletal system (body structure)	false	Inferred relationship	Some
Autosomal dominant epidermolysis bullosa simplex	Finding site	Connective tissue structure	false	Inferred relationship	Some
Autosomal dominant epidermolysis bullosa simplex	Associated morphology	Congenital anomaly	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)