Autosomal dominant Alzheimer disease due to mutation of presenilin 2 1156798001

SNOMED CT code

SNOMED code

1156798001

name

Autosomal dominant Alzheimer disease due to mutation of presenilin 2

status

active

date introduced

2021-07-31

fully specified name(s)

Autosomal dominant Alzheimer disease due to mutation of presenilin 2 (disorder)

synonyms

Autosomal dominant Alzheimer disease with mutation of presenilin 2
Autosomal dominant Alzheimer disease due to mutation of presenilin 2

attributes - group1

Associated morphology

Degenerative abnormality 107669003

Finding site

Cerebrum 83678007

attributes - group2

Interprets

Cognitive functions 311465003

Has interpretation

Impaired 260379002

parents

Hereditary degenerative disease of central nervous system 106018006
Autosomal dominant hereditary disorder 11164009
Familial Alzheimer's disease of early onset 230265002

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Degenerative disorder 362975008
Degenerative disease of the central nervous system 80690008
Hereditary degenerative disease of central nervous system 106018006
Autosomal dominant Alzheimer disease due to mutation of presenilin 2 1156798001

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal dominant hereditary disorder 11164009
Autosomal dominant Alzheimer disease due to mutation of presenilin 2 1156798001

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Familial disease 111941005
Familial Alzheimer's disease of early onset 230265002
Autosomal dominant Alzheimer disease due to mutation of presenilin 2 1156798001

ancestors

sorted most to least specific

Hereditary degenerative disease of central nervous system 106018006
Autosomal dominant hereditary disorder 11164009
Familial Alzheimer's disease of early onset 230265002
Hereditary disorder of nervous system 363235000
Autosomal hereditary disorder 1899006
Familial disease 111941005
Primary degenerative dementia of the Alzheimer type, presenile onset 416780008
Hereditary disorder by system 363137000
Presenile dementia 12348006
Alzheimer's disease 26929004
Hereditary disease 32895009
Dementia 52448006
Cerebral degeneration presenting primarily with dementia 279982005
Genetic disease 782964007
Organic mental disorder 111479008
Cerebral degeneration 418143002
Impaired cognition 386806002
Mental disorder 74732009
Degenerative brain disorder 52522001
Cognitive function finding 373930000
Degenerative disease of the central nervous system 80690008
Functional finding 118228005
Disorder of brain 81308009
Disorder of the central nervous system 23853001
Degenerative disorder 362975008
Disorder of head 118934005
Finding of brain 299718000
Disorder of nervous system 118940003
Central nervous system finding 246556002
Head finding 406122000
Disorder of body system 362965005
Finding of head and neck region 118254002
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:

CPT® to SNOMED Crosswalks

Thank you for choosing Find-A-Code, please Sign In to remove ads.

MY NEWSLETTERS

FEES

FACILITY

RISK ADJUSTMENT

SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Degenerative disorder 362975008

Degenerative disease of the central nervous system 80690008

Hereditary degenerative disease of central nervous system 106018006

Autosomal dominant Alzheimer disease due to mutation of presenilin 2 1156798001

SNOMED CT code