Diagnosis final clinical death type

General Details:

Name:
Diagnosis final clinical death type
Steward:
NINDS
Definition:
Physician's final clinical diagnosis for the participant/subject
Registration Status:
Qualified

Permissible Values:

Data Type:
Value List
Unit of Measure:
Ids:
Value Code Name Code Code System Code Description
Multiple system atrophy Multiple system atrophy Multiple system atrophy
Progressive supranuclear palsy Progressive supranuclear palsy Progressive supranuclear palsy
Corticobasal degeneration Corticobasal degeneration Corticobasal degeneration
Other, specify Other, specify Other, specify
Chorea gravidarum Chorea gravidarum Chorea gravidarum
Dentato-rubro-pallido-luysian atrophy (DRPLA), with genetically confirmed expansion of CAG repeats Dentato-rubro-pallido-luysian atrophy (DRPLA), with genetically confirmed expansion of CAG repeats Dentato-rubro-pallido-luysian atrophy (DRPLA), with genetically confirmed expansion of CAG repeats
Dentato-rubro-pallido-luysian atrophy (DRPLA), without genetically confirmed expansion of CAG repeats Dentato-rubro-pallido-luysian atrophy (DRPLA), without genetically confirmed expansion of CAG repeats Dentato-rubro-pallido-luysian atrophy (DRPLA), without genetically confirmed expansion of CAG repeats
Fragile X syndrome with genetically confirmed expansion of CGG repeats Fragile X syndrome with genetically confirmed expansion of CGG repeats Fragile X syndrome with genetically confirmed expansion of CGG repeats
Fragile X syndrome without genetically confirmed expansion of CGG repeats Fragile X syndrome without genetically confirmed expansion of CGG repeats Fragile X syndrome without genetically confirmed expansion of CGG repeats
Friedreich ataxia with genetically confirmed expansion of GAA repeats Friedreich ataxia with genetically confirmed expansion of GAA repeats Friedreich ataxia with genetically confirmed expansion of GAA repeats
Friedreich ataxia without genetically confirmed expansion of GAA repeats Friedreich ataxia without genetically confirmed expansion of GAA repeats Friedreich ataxia without genetically confirmed expansion of GAA repeats
Frontotemporal lobar degeneration Frontotemporal lobar degeneration Frontotemporal lobar degeneration
Hepatolenticular degeneration or Wilson disease Hepatolenticular degeneration or Wilson disease Hepatolenticular degeneration or Wilson disease
Huntington disease with genetically confirmed expansion of HD-IT15 CAG repeats Huntington disease with genetically confirmed expansion of HD-IT15 CAG repeats Huntington disease with genetically confirmed expansion of HD-IT15 CAG repeats
Huntington disease without genetically confirmed expansion of HD-IT15 CAG repeats Huntington disease without genetically confirmed expansion of HD-IT15 CAG repeats Huntington disease without genetically confirmed expansion of HD-IT15 CAG repeats
Huntington disease-like 2 genetically confirmed expansion of trinucleotide repeats Huntington disease-like 2 genetically confirmed expansion of trinucleotide repeats Huntington disease-like 2 genetically confirmed expansion of trinucleotide repeats
Huntington disease-like without genetically confirmed expansion of trinucleotide repeats Huntington disease-like without genetically confirmed expansion of trinucleotide repeats Huntington disease-like without genetically confirmed expansion of trinucleotide repeats
Kennedy disease with genetically confirmed expansion of CAG repeats Kennedy disease with genetically confirmed expansion of CAG repeats Kennedy disease with genetically confirmed expansion of CAG repeats
Kennedy disease without genetically confirmed expansion of CAG repeats Kennedy disease without genetically confirmed expansion of CAG repeats Kennedy disease without genetically confirmed expansion of CAG repeats
Pantothenate kinase-associated neurodegeneration (Hallervorden-Spatz syndrome) Pantothenate kinase-associated neurodegeneration (Hallervorden-Spatz syndrome) Pantothenate kinase-associated neurodegeneration (Hallervorden-Spatz syndrome)
Senile chorea or vascular chorea Senile chorea or vascular chorea Senile chorea or vascular chorea
Spinocerebellar ataxia with genetically confirmed expansion of either CAG or CTG repeats Spinocerebellar ataxia with genetically confirmed expansion of either CAG or CTG repeats Spinocerebellar ataxia with genetically confirmed expansion of either CAG or CTG repeats
Spinocerebellar ataxia without genetically confirmed expansion of either CAG or CTG repeats Spinocerebellar ataxia without genetically confirmed expansion of either CAG or CTG repeats Spinocerebellar ataxia without genetically confirmed expansion of either CAG or CTG repeats
Subacute sclerosing panencephalitis Subacute sclerosing panencephalitis Subacute sclerosing panencephalitis
Sydenham chorea Sydenham chorea Sydenham chorea
Tardive dyskinesia Tardive dyskinesia Tardive dyskinesia
Neuroacanthocytosis Neuroacanthocytosis Neuroacanthocytosis
Pick disease Pick disease Pick disease

Designations:

Designation:
Diagnosis final clinical death type
Tags:

Designations:

Definition:
Physician's final clinical diagnosis for the participant/subject
Tags:

Identifiers:

Source:
NLM
Id:
2OS_2xyQjKs
Version:
3.1
Source:
NINDS
Id:
C08149
Version:
3
Source:
BRICS Variable Name
Id:
DiagnosFinalClinDeathTyp
Version: