192784006: Metachromatic leucodystrophy (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module

296972018 Metachromatic leukodystrophy en Synonym Active Entire term case insensitive SNOMED CT core module

296973011 Sulphatide lipidosis en Synonym Active Entire term case insensitive SNOMED CT core module

296974017 Sulfatide lipidosis en Synonym Active Entire term case insensitive SNOMED CT core module

296975016 Greenfield disease en Synonym Active Entire term case sensitive SNOMED CT core module

296976015 Metachromatic leucodystrophy en Synonym Active Entire term case insensitive SNOMED CT core module

296977012 MLD en Synonym Active Entire term case sensitive SNOMED CT core module

296978019 Familial progressive cerebral sclerosis en Synonym Active Entire term case insensitive SNOMED CT core module

296979010 van Bogaert-Nijssen disease en Synonym Active Entire term case sensitive SNOMED CT core module

296980013 MLD - Metachromatic leucodystrophy en Synonym Active Entire term case sensitive SNOMED CT core module

296981012 Metachromatic leukoencephaly en Synonym Active Entire term case insensitive SNOMED CT core module

576603011 Metachromatic leucodystrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Metachromatic leucodystrophy	Is a	Sphingolipidosis	false	Inferred relationship	Existential restriction modifier
Metachromatic leucodystrophy	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Metachromatic leucodystrophy	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier

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

This concept is not in any reference sets