Neurology Dataset

Neurological Phenotype Registry

Research-grade neurological phenotype dataset with structured clinical phenotyping, imaging metadata, and biofluid biomarker data for CNS disease research. Designed with HIPAA Safe Harbor de-identification standards, with full consent chain documentation for licensing.

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Dataset specifications

This registry covers CNS disease phenotyping cohorts with structured clinical phenotype records, neuroimaging acquisition metadata, standardized cognitive assessment scores, and biofluid biomarker data (CSF and plasma panels where available). Longitudinal follow-up up to 36 months. Applicable to neurodegenerative disease progression modeling, epilepsy subtype characterization, and cognitive decline biomarker validation. All records are de-identified per HIPAA Safe Harbor method, QC-validated, and consent-verified before catalog inclusion.

Available modalities

Structured clinical phenotypes
Neuroimaging metadata
Cognitive assessments
Biofluid biomarkers

Common research indications

Neurodegenerative disease
Epilepsy phenotyping
Cognitive decline biomarkers

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Dataset metadata

Sample range600–2,100 subjects

De-identificationHIPAA Safe Harbor (18 identifiers)

Consent modelBroad consent

Primary modalitiesPhenotypic / Clinical / Imaging

Follow-up durationUp to 36 months

FormatFHIR R4, Parquet, CSV

Last updatedQ4 2025

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