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1156789004: Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4576192011 Autosomal dominant Alzheimer disease with mutation of amyloid precursor protein en Synonym Active Only initial character case insensitive SNOMED CT core module
4576910017 Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein en Synonym Active Only initial character case insensitive SNOMED CT core module
4576911018 Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein Has interpretation Impaired true Inferred relationship Existential restriction modifier 2
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein Interprets Cognitive functions true Inferred relationship Existential restriction modifier 2
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein Is a Familial Alzheimer's disease of early onset true Inferred relationship Existential restriction modifier
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein Finding site Structure of cerebrum true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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