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1003375005: Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4168107010 Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
4168108017 Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency Is a Metachromatic leucodystrophy true Inferred relationship Existential restriction modifier
Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency Due to Sphingolipid activator protein 1 deficiency true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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