Name Steward Organization Suggested Domain Suggested Domain Description Cde Group Classification
Diagnosis final clinical death type NINDS Disease characterization
Including Alzheimer's Disease (AD)/AD-Related Dementias (ADRD) diagnosis and multiple chronic conditions (MCCs)
 NIH CDEs
  • ▼ NINDS
    • ▼ Disease
      • ▼ Huntington’s Disease
        • ▼ Classification
          • Supplemental
        • ▼ Domain
          • ▼ Assessments and Examinations
            • Other Clinical Data
      • ▼ Parkinson's Disease
        • ▼ Classification
          • Supplemental
        • ▼ Domain
          • ▼ Assessments and Examinations
            • Other Clinical Data
    • ▼ Domain
      • ▼ Assessments and Examinations
        • Other Clinical Data
    • ▼ Population
      • Adult

# Datatype

UUID: d1381b64-eb6d-5910-91f6-0268b773eff8

Value List

# Permissible value Value meaning name Value meaning definition

UUID: b21242af-dffa-5a16-a478-c6681aa92c69

Chorea gravidarum Chorea gravidarum Chorea gravidarum

UUID: ba2652d7-1649-52e0-8ae7-0249b90c7dea

Corticobasal degeneration Corticobasal degeneration Corticobasal degeneration

UUID: aead0a71-1cb0-51ad-b1f9-6a793045b744

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

UUID: 74eb88fa-d4c6-5bea-9175-4b06de03de38

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

UUID: e6cb2714-7600-51ad-84b4-cc2925d63b74

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

UUID: 09386c46-8337-557c-a050-650304adbbd3

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

UUID: afdbc003-b7d3-50f7-b2df-1b339c436aaf

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

UUID: 4102b8fb-a2bd-520e-b36e-ce7fe8df2bff

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

UUID: aa47e63d-fe96-5b88-b406-625c15555c74

Frontotemporal lobar degeneration Frontotemporal lobar degeneration Frontotemporal lobar degeneration

UUID: b26be55e-9e86-5d0b-aa1e-df0236c91ddf

Hepatolenticular degeneration or Wilson disease Hepatolenticular degeneration or Wilson disease Hepatolenticular degeneration or Wilson disease

UUID: e7d4aa73-d4e8-5d5c-b446-0ccbb4cdcf37

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

UUID: 1f55c2b7-b940-5a80-91ec-dbb47d452842

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

UUID: 2f07dea0-1047-59da-8022-63be1e015bcb

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

UUID: a76aa5ea-a8af-501a-8646-c33999d74f3b

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

UUID: 4a38b69d-8840-5b11-a78e-fd1ced36433b

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

UUID: f3b54110-ce52-558d-b486-966511a642a6

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

UUID: 73a52c12-4489-569a-97bb-b122e6dee435

Multiple system atrophy Multiple system atrophy Multiple system atrophy

UUID: 674c06af-f823-5ed1-90dc-c30fd2233b56

Neuroacanthocytosis Neuroacanthocytosis Neuroacanthocytosis

UUID: ab598550-77a6-57ba-8c72-553513513d24

Other, specify Other, specify Other, specify

UUID: 5b959b2c-df88-55a8-b9f5-8569d04c064a

Pantothenate kinase-associated neurodegeneration (Hallervorden-Spatz syndrome) Pantothenate kinase-associated neurodegeneration (Hallervorden-Spatz syndrome) Pantothenate kinase-associated neurodegeneration (Hallervorden-Spatz syndrome)

UUID: 83590897-4d6c-5a7b-a2ca-c4c2b35ed50a

Pick disease Pick disease Pick disease

UUID: 8da76202-adc2-553e-82d1-8c6c12801bc6

Progressive supranuclear palsy Progressive supranuclear palsy Progressive supranuclear palsy

UUID: 2dde21d6-4d19-5c06-be9a-890b0e204c46

Senile chorea or vascular chorea Senile chorea or vascular chorea Senile chorea or vascular chorea

UUID: a33fc301-ac29-5cd0-b6e8-820dc33077f1

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

UUID: a986eec9-4913-5ce3-9110-2e30eba000f4

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

UUID: 04c0b99a-3324-5e0c-9382-a2fe546a5517

Subacute sclerosing panencephalitis Subacute sclerosing panencephalitis Subacute sclerosing panencephalitis

UUID: 606d2f15-7fe6-5547-8203-091278b7bb1b

Sydenham chorea Sydenham chorea Sydenham chorea

UUID: 1e570ab9-75b6-5b84-b810-c029a6e06a63

Tardive dyskinesia Tardive dyskinesia Tardive dyskinesia

# Definition

UUID: 05acd7e6-a529-5176-bb31-5397d260f640

Physician's final clinical diagnosis for the participant/subject

# Designation

UUID: 98754493-91a5-5c42-92ac-552da7cbcfd6

Diagnosis final clinical death type

# Identifier Origin Version

UUID: 631dd528-d6eb-5b50-a171-77baca54e505

C08149 NINDS 3

UUID: dd2d8813-f383-58a4-93ea-39cfaca117c1

DiagnosFinalClinDeathTyp BRICS Variable Name N/A

UUID: 4abf5534-b729-5b47-b5c4-239a34454e68

2OS_2xyQjKs NLM CDEs 12-02-2025-download