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733422008: Prion protein systemic amyloidosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3499403010 Prion protein systemic amyloidosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3499404016 Chronic diarrhoea with hereditary sensory and autonomic neuropathy en Synonym Active Entire term case insensitive SNOMED CT core module
3499405015 Prion protein systemic amyloidosis en Synonym Active Entire term case insensitive SNOMED CT core module
3499406019 PrP (prion protein) systemic amyloidosis en Synonym Active Entire term case sensitive SNOMED CT core module
3499407011 Chronic diarrhea with hereditary sensory and autonomic neuropathy en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Prion protein systemic amyloidosis Associated morphology Amyloid deposition true Inferred relationship Existential restriction modifier 1
Prion protein systemic amyloidosis Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Prion protein systemic amyloidosis Is a Prion disease true Inferred relationship Existential restriction modifier
Prion protein systemic amyloidosis Is a Systemic amyloidosis true Inferred relationship Existential restriction modifier
Prion protein systemic amyloidosis Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Prion protein systemic amyloidosis Associated morphology Spongy degeneration true Inferred relationship Existential restriction modifier 2
Prion protein systemic amyloidosis Causative agent Prion true Inferred relationship Existential restriction modifier 2
Prion protein systemic amyloidosis Finding site Brain tissue structure true Inferred relationship Existential restriction modifier 2
Prion protein systemic amyloidosis Pathological process Infectious process true Inferred relationship Existential restriction modifier 2
Prion protein systemic amyloidosis Is a Hereditary amyloidosis true Inferred relationship Existential restriction modifier
Prion protein systemic amyloidosis Is a Hereditary degenerative disease of central nervous system 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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