Dentatorubropallidoluysian degeneration 68116008

SNOMED CT code

SNOMED code

68116008

name

Dentatorubropallidoluysian degeneration

status

active

date introduced

2002-01-31

fully specified name(s)

Dentatorubropallidoluysian degeneration (disorder)

synonyms

Dentatorubropallidoluysian degeneration
Dentatorubropallidoluysian atrophy
DRPLA - Dentatorubropallidoluysian atrophy
Dentatorubral-pallidoluysian atrophy
Dentatorubral-pallidoluysian atrophy (DRPLA)
Naito-Oyanagi disease
Haw river syndrome
Myoclonic epilepsy with choreoathetosis

attributes - group2

Has interpretation

Abnormal 263654008

Interprets

Movement observable 363847004

attributes - group3

Finding site

Basal ganglion structure 32610002

attributes - group4

Interprets

Movement 255324009

attributes - group1

Finding site

Cerebellar structure 113305005

parents

Autosomal dominant hereditary disorder 11164009
Chorea 271700006
Hereditary ataxia 763597000
Cerebellar ataxia 85102008

children

Chorea co-occurrent and due to dentatorubropallidoluysian degeneration 724765008

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal dominant hereditary disorder 11164009
Dentatorubropallidoluysian degeneration 68116008

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of movement 298325004
Involuntary movement 267078001
Chorea 271700006
Dentatorubropallidoluysian degeneration 68116008

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of coordination 298314008
Ataxia 20262006
Hereditary ataxia 763597000
Dentatorubropallidoluysian degeneration 68116008

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of coordination 298314008
Ataxia 20262006
Cerebellar ataxia 85102008
Dentatorubropallidoluysian degeneration 68116008

ancestors

sorted most to least specific

Autosomal dominant hereditary disorder 11164009
Chorea 271700006
Hereditary ataxia 763597000
Cerebellar ataxia 85102008
Autosomal hereditary disorder 1899006
Involuntary movement 267078001
Ataxia 20262006
Disorder of basal ganglia 70835005
Extrapyramidal disease 76349003
Hereditary disorder of nervous system 363235000
Cerebellar disorder 223176004
Finding of coordination 298314008
Finding of head region 298364001
Movement disorder 60342002
Disorder of brain 81308009
Hereditary disorder by system 363137000
Hereditary disease 32895009
Finding of movement 298325004
Disorder of head 118934005
Disorder of the central nervous system 23853001
Finding of brain 299718000
Genetic disease 782964007
Head finding 406122000
Disorder of nervous system 118940003
Central nervous system finding 246556002
Finding of head and neck region 118254002
Disorder of body system 362965005
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

Genetic disease 782964007

Hereditary disease 32895009

Autosomal hereditary disorder 1899006

Autosomal dominant hereditary disorder 11164009

Dentatorubropallidoluysian degeneration 68116008

SNOMED CT code