FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

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


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

Descriptions:

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


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 Some 2
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein Is a Hereditary degenerative disease of central nervous system true Inferred relationship Some
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein Interprets Cognitive functions true Inferred relationship Some 2
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein Is a Familial Alzheimer's disease of early onset true Inferred relationship Some
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein Finding site Cerebrum true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

Back to Start