192784006: Metachromatic leucodystrophy (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

296972018 Metachromatic leukodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

296973011 Sulphatide lipidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

296974017 Sulfatide lipidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

296975016 Greenfield disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

296976015 Metachromatic leucodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

296977012 MLD en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

296978019 Familial progressive cerebral sclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

296979010 van Bogaert-Nijssen disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

296980013 MLD - Metachromatic leucodystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

296981012 Metachromatic leukoencephaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

576603011 Metachromatic leucodystrophy (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
Metachromatic leucodystrophy	Is a	Sphingolipidosis	false	Inferred relationship	Some
Metachromatic leucodystrophy	Finding site	Body system structure	false	Inferred relationship	Some
Metachromatic leucodystrophy	Occurrence	Congenital	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Arylsulfatase A deficiency	Is a	False	Metachromatic leucodystrophy	Inferred relationship	Some
Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator	Is a	False	Metachromatic leucodystrophy	Inferred relationship	Some
Metachromatic leukodystrophy, congenital type	Is a	False	Metachromatic leucodystrophy	Inferred relationship	Some
Sphingolipid activator protein 1 deficiency	Is a	False	Metachromatic leucodystrophy	Inferred relationship	Some
Metachromatic leukodystrophy without arylsulfatase deficiency	Is a	False	Metachromatic leucodystrophy	Inferred relationship	Some

Reference Sets

Concept inactivation indicator reference set

Description inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)