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66751000: Niemann-Pick disease, type C (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
110890015 Niemann-Pick disease, type C en Synonym Active Entire term case sensitive SNOMED CT core module
500515016 Supraoptic vertical ophthalmoplegia en Synonym Active Entire term case insensitive SNOMED CT core module
500516015 Niemann-Pick disease type C en Synonym Active Entire term case sensitive SNOMED CT core module
806399018 Niemann-Pick disease, type C (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


3 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Niemann-Pick disease, type C, subacute form Is a True Niemann-Pick disease, type C Inferred relationship Existential restriction modifier
Niemann-Pick disease, type C, chronic form Is a True Niemann-Pick disease, type C Inferred relationship Existential restriction modifier
Niemann-Pick disease, type C, acute form Is a True Niemann-Pick disease, type C Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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