56096001: Facioscapulohumeral muscular dystrophy (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

93289013 Fascioscapulohumeral muscular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

93290016 Landouzy-Dejerine muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

93291017 Landouzy-Déjérine muscular dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

93292012 Facioscapulohumeral muscular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

93293019 Limb-girdle muscular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

497510015 FSH - Facioscapulohumeral muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

497511016 FMD - Facioscapulohumeral muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

497512011 FSHD - Facioscapulohumeral muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

794570010 Facioscapulohumeral muscular dystrophy (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
Facioscapulohumeral muscular dystrophy	Is a	Autosomal dominant muscular dystrophy not predominantly limb girdle	false	Inferred relationship	Some
Facioscapulohumeral muscular dystrophy	Finding site	Skeletal muscle structure	false	Inferred relationship	Some
Facioscapulohumeral muscular dystrophy	Occurrence	Congenital	false	Inferred relationship	Some
Facioscapulohumeral muscular dystrophy	Associated morphology	kongenital anomali	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set (foundation metadata concept)