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58459009: Sphingomyelin/cholesterol lipidosis (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
97145019 Sphingomyelin/cholesterol lipidosis en Synonym Active Entire term case insensitive SNOMED CT core module
97146018 Neuronal cholesterol lipidosis en Synonym Active Entire term case insensitive SNOMED CT core module
97149013 Sphingomyelinase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
97154016 Niemann-Pick disease en Synonym Active Entire term case sensitive SNOMED CT core module
97155015 Sphingomyelin lipidosis en Synonym Active Entire term case insensitive SNOMED CT core module
797193019 Sphingomyelin/cholesterol lipidosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

7 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Sphingomyelin/cholesterol lipidosis Is a Lipoidosis true Inferred relationship Existential restriction modifier
Sphingomyelin/cholesterol lipidosis Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Sphingomyelin/cholesterol lipidosis Is a Lipid storage disease true Inferred relationship Existential restriction modifier
Sphingomyelin/cholesterol lipidosis Is a Sphingolipidosis true Inferred relationship Existential restriction modifier
Sphingomyelin/cholesterol lipidosis Associated morphology Niemann-Pick cell false Inferred relationship Existential restriction modifier
Sphingomyelin/cholesterol lipidosis Associated morphology Foam cell false Inferred relationship Existential restriction modifier
Sphingomyelin/cholesterol lipidosis Finding site Body system structure false Inferred relationship Existential restriction modifier
Sphingomyelin/cholesterol lipidosis Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Niemann-Pick disease, type D Is a True Sphingomyelin/cholesterol lipidosis Inferred relationship Existential restriction modifier
Niemann-Pick disease, type B Is a True Sphingomyelin/cholesterol lipidosis Inferred relationship Existential restriction modifier
Niemann-Pick disease, type A Is a True Sphingomyelin/cholesterol lipidosis Inferred relationship Existential restriction modifier
Niemann-Pick disease, type C Is a True Sphingomyelin/cholesterol lipidosis Inferred relationship Existential restriction modifier
Niemann-Pick disease, type E Is a False Sphingomyelin/cholesterol lipidosis Inferred relationship Existential restriction modifier
Cerebral degeneration in Niemann-Pick disease Due to True Sphingomyelin/cholesterol lipidosis Inferred relationship Existential restriction modifier 2

This concept is not in any reference sets

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