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870313002: Perinatal lethal Gaucher disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3968883014 Perinatal lethal Gaucher disease (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3968884015 Perinatal lethal Gaucher disease 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
Perinatal lethal Gaucher disease Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Perinatal lethal Gaucher disease Is a Glucosylceramide beta-glucosidase deficiency true Inferred relationship Existential restriction modifier
Perinatal lethal Gaucher disease Is a Perinatal disorder false Inferred relationship Existential restriction modifier
Perinatal lethal Gaucher disease Occurrence Perinatal period false Inferred relationship Existential restriction modifier 1
Perinatal lethal Gaucher disease Occurrence Perinatal period of fetus and/or neonate true Inferred relationship Existential restriction modifier 1
Perinatal lethal Gaucher disease Is a Perinatal endocrine and metabolic disorders true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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