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1156798001: Autosomal dominant Alzheimer disease due to mutation of presenilin 2 (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
4576210013 Autosomal dominant Alzheimer disease with mutation of presenilin 2 en Synonym Active Only initial character case insensitive SNOMED CT core module
4576890017 Autosomal dominant Alzheimer disease due to mutation of presenilin 2 (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
4576891018 Autosomal dominant Alzheimer disease due to mutation of presenilin 2 en Synonym 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 presenilin 2 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Autosomal dominant Alzheimer disease due to mutation of presenilin 2 Interprets Cognitive functions true Inferred relationship Existential restriction modifier 2
Autosomal dominant Alzheimer disease due to mutation of presenilin 2 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant Alzheimer disease due to mutation of presenilin 2 Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
Autosomal dominant Alzheimer disease due to mutation of presenilin 2 Has interpretation Impaired true Inferred relationship Existential restriction modifier 2
Autosomal dominant Alzheimer disease due to mutation of presenilin 2 Is a Familial Alzheimer's disease of early onset true Inferred relationship Existential restriction modifier
Autosomal dominant Alzheimer disease due to mutation of presenilin 2 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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