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39390005: Niemann-Pick disease, type B (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
66053013 Niemann-Pick disease, type B en Synonym Active Entire term case sensitive SNOMED CT core module
66054019 Niemann-Pick disease, chronic non-neuronopathic en Synonym Active Entire term case sensitive SNOMED CT core module
775833011 Niemann-Pick disease, type B (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1229519010 Niemann-Pick disease type B en Synonym Active Entire term case sensitive SNOMED CT core module
1229520016 Niemann-Pick disease non-neuropathic type en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Niemann-Pick disease, type B Is a Sphingomyelin/cholesterol lipidosis true Inferred relationship Existential restriction modifier
Niemann-Pick disease, type B Associated morphology Niemann-Pick cell false Inferred relationship Existential restriction modifier
Niemann-Pick disease, type B Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Niemann-Pick disease, type B Finding site Body system structure false Inferred relationship Existential restriction modifier
Niemann-Pick disease, type B Associated morphology Foam cell false 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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