CDE Catalog

***Please contact the NINDS CDE Team (NINDSCDE@emmes.com) if you encounter any search difficulties.***

The CDE Catalog is a directory of the available NINDS CDEs. Users can search the Catalog to isolate a subset of the CDEs (e.g., all stroke-specific CDEs, etc.), and to view and download details about the CDEs.

Select any filter below to search the CDE Catalog.

For best results, clear form between searches. In addition, when specifying NeuroRehab, Sport-Related Concussion (SRC) or Traumatic Brain Injury (TBI) as the Disease, please select a Subdisease as well.

NeuroRehab Comprehensive includes all NeuroRehab CDE recommendations. NeuroRehab General includes all NeuroRehab CDE recommendations that are not disease specific. All other NeuroRehab Subdiseases include recommendations specific to existing NINDS CDE project disorders.

Choose your Time Frame for your SRC study (Acute (time of injury until 72 hours), Subacute (after 72 hours to 3 months), and Persistent/Chronic (3 months and greater post-concussion) or Comprehensive if your study falls across the study time frames.

Choose your type of TBI study (Acute Hospitalized, Concussion/Mild TBI, Moderate/Severe TBI: Rehabilitation, or Epidemiology) or Comprehensive if your study falls outside of the study types or incorporates aspects of more than one type of study.

Search Form

Displaying 301 - 325 of 1249
Operations
Selected 25 rows in this page.  
The search results below can be downloaded by clicking the checkboxes on the far left side of the table. Select the header checkbox to select all CDEs listed on the first page. Then choose CDE Detailed Report from the Choose an operation dropdown menu.
CDE ID CDE Name Definition Classification CRF Name Copyrighted or trademarked Disease Name Subdisease Name
C59197 Gait stride length barefoot condition right measurement

Value of the distance in meters from heel contact to heel contact on the right foot in the barefoot condition

Supplemental-Highly Recommended Gait Analysis Cerebral Palsy Cerebral Palsy
C59205 Gait stride length orthotic condition left measurement

Value of the distance measured in meters from heel contact to heel contact on the left foot in the orthotic condition

Supplemental-Highly Recommended Gait Analysis Cerebral Palsy Cerebral Palsy
C59206 Gait stride length orthotic condition right measurement

Value of the distance measured in meters from heel contact to heel contact on the right foot in the orthotic condition

Supplemental-Highly Recommended Gait Analysis Cerebral Palsy Cerebral Palsy
C59194 Gait velocity barefoot condition measurement

Value of the speed measured in meters per second in the barefoot condition

Supplemental-Highly Recommended Gait Analysis Cerebral Palsy Cerebral Palsy
C59203 Gait velocity orthotic condition measurement

Value of the speed measured in meters per second in the orthotic condition

Supplemental-Highly Recommended Gait Analysis Cerebral Palsy Cerebral Palsy
C12208 Gastrointestinal therapy nutrition supplement type

Type(s) of nutritional supplement(s) being taken by the participant/subject

Supplemental Medical History Cerebral Palsy Cerebral Palsy
C12207 Gastrointestinal therapy take nutrition supplement indicator

Indicator whether the participant/subject is taking nutritional supplements

Supplemental Medical History Cerebral Palsy Cerebral Palsy
C58677 Gender identity type

Gender identity self-identified by the subject/participant. Gender type may or may not match sex assigned at birth

Core General Core Cerebral Palsy Cerebral Palsy
C58781 Gender identity type other text

The free-text field related to 'Gender identity type', specifying other text

Supplemental General Core Cerebral Palsy Cerebral Palsy
C00035 Gender type

Self-reported gender of the participant/subject

Supplemental Behavioral Rating Inventory of Executive Function - Adult Version (BRIEF-A) Cerebral Palsy Cerebral Palsy
C00035 Gender type

Self-reported gender of the participant/subject

Supplemental Wechsler Abbreviated Scale of Intelligence - Second Edition (WASI-II) Cerebral Palsy Cerebral Palsy
C00035 Gender type

Self-reported gender of the participant/subject

Core Demographics Cerebral Palsy Cerebral Palsy
C00035 Gender type

Self-reported gender of the participant/subject

Supplemental Test of Everyday Attention for Children (TEA-Ch) Cerebral Palsy Cerebral Palsy
C12782 Gene additional variants unknown significance indicator

Whether there are additional variants in other genes of unknown significance

Supplemental-Highly Recommended Mutation Analysis Cerebral Palsy Cerebral Palsy
C17891 Gene additional variants unknown significance text

Text about additional variants in other genes of unknown significance

Supplemental Mutation Analysis Cerebral Palsy Cerebral Palsy
C12804 Gene cDNA variant or mutation name

The Human Genome Organisation (HUGO) variant or mutation nomenclature of the complementary deoxyribonucleic acid (cDNA) variant or mutation

Supplemental Mutation Analysis Cerebral Palsy Cerebral Palsy
C12795 Gene coding region sequenced indicator

For missense/nonsense variant or point mutations or pseudoexons, whether the entire coding region was sequenced for the allele of the gene

Supplemental Mutation Analysis Cerebral Palsy Cerebral Palsy
C12789 Gene deletions duplications limits clearly defined indicator

Whether the limits of deletions and duplications are defined

Supplemental Mutation Analysis Cerebral Palsy Cerebral Palsy
C12788 Gene exon copy number tested indicator

Whether the copy number was directly tested for all exons

Supplemental Mutation Analysis Cerebral Palsy Cerebral Palsy
C12790 Gene exon first deleted duplicated name

Identify first exon deleted or duplicated

Supplemental Mutation Analysis Cerebral Palsy Cerebral Palsy
C12791 Gene exon last deleted duplicated name

Identify exon last deleted or duplicated

Supplemental Mutation Analysis Cerebral Palsy Cerebral Palsy
C12793 Gene exon predicted reading frame type

Type of predicted reading frame

Supplemental Mutation Analysis Cerebral Palsy Cerebral Palsy
C12800 Gene missense nonsense variant or point mutation insertion deletion type

The insertion deletion type of the missense/nonsense variant or point mutation

Supplemental Mutation Analysis Cerebral Palsy Cerebral Palsy
C17889 Gene missense nonsense variant or point mutation location exon text

Text about missense/nonsense variant or point mutation at the exon

Supplemental Mutation Analysis Cerebral Palsy Cerebral Palsy
C17894 Gene missense nonsense variant or point mutation location intron text

Text about missense/nonsense variant or point mutation at the intron

Supplemental Mutation Analysis Cerebral Palsy Cerebral Palsy
Displaying 301 - 325 of 1249

The NINDS CDE Team does not post proprietary instruments/scales recommended by the CDE Working Groups on this website. This includes, but is not limited to, copyrighted or trademarked instruments/scales. Information about recommended instruments can be found in the Notice of Copyright (NOC) documents under ‘CRF Module/Guideline’ on each disorder’s data standards page. For any questions regarding these instruments/scales please contact the corresponding owner/author. The NINDS CDE Team is not responsible for the availability or content of these external sites, nor does the NINDS CDE Team endorse, warrant or guarantee the products, services or information described or offered at these other internet sites.