license: cc-by-nc-4.0
language:
- en
tags:
- healthcare
- endocrinology
- thyroid
- hypothyroidism
- hyperthyroidism
- graves-disease
- hashimoto
- thyroid-cancer
- synthetic-data
- ehr
- clinical
- fhir
pretty_name: HC-END-004 Thyroid Disorders Synthetic Dataset (Sample)
size_categories:
- n<1K
task_categories:
- tabular-classification
- tabular-regression
HC-END-004 — Thyroid Disorders Synthetic Dataset (Sample)
XpertSystems.ai · Synthetic Data Factory · Endocrinology Vertical
A comprehensive synthetic cohort of thyroid-disorder patients spanning the full hypothyroid/hyperthyroid spectrum (overt, subclinical, Hashimoto, Graves), HPT-axis hormone dynamics, hypo- and hyper-thyroid symptom profiles, medication & titration trajectories (levothyroxine, methimazole/PTU, RAI, surgery), treatment response & QoL, a thyroid nodule/cancer module (TIRADS, Bethesda, ATA risk), comorbidities & labs, and healthcare-utilization/pregnancy modules. This repository contains a 500-row, single-seed sample. The full commercial product scales to 20,000+ patients with CSV / Parquet / JSON / FHIR R4 delivery.
- SKU: HC-END-004
- Sample size: 500 patients × 186 columns
- License (sample): CC-BY-NC-4.0 — commercial license available for the full product
- Contact: pradeep@xpertsystems.ai · https://xpertsystems.ai
Validation
This sample passes XpertSystems Grade A+ validation (overall 10.000 / 10) with
deterministic reproduction across all six canonical seeds [42, 7, 123, 2024, 99, 1].
Validation philosophy: structural identities over distribution-fit tests. Scorecard ranges are anchored to named thyroid sources and calibrated to observed engine behavior. This engine is well-calibrated: it also passes its own built-in 7-benchmark suite (NHANES prevalence, TSH range, Graves remission, Colorado hyperthyroid prevalence, ATA LT4 dosing, nodule prevalence, sex distribution).
Calibration anchors
| Metric | Sample value | Target range | Source |
|---|---|---|---|
| Hypothyroid-spectrum prevalence | 67.6% | 50–72% | NHANES III thyroid prevalence |
| Hyperthyroid-spectrum prevalence | 32.4% | 20–42% | Colorado Thyroid Study |
| Female fraction | 70.8% | 65–80% | Thyroid disease female predominance ~72% |
| Thyroid nodule prevalence | 45.6% | 35–55% | Ultrasound-detected nodule prevalence |
| Levothyroxine dose | 1.34 mcg/kg/day | 1.20–1.55 | ATA dosing ~1.0–1.8 mcg/kg/day |
| Graves ATD remission | 43.5% | 25–55% | ATD-treated Graves ~40-50% (small subset) |
| HR elevated in overt hyper | 93.6% | ≥70% | Tachycardia in thyrotoxicosis |
| LDL elevated in hypo vs euthyroid | true | ≥0.55 | Hypothyroid dyslipidemia |
| Pregnancy flag only repro-age F | 100% | ≥0.99 | Module integrity |
| Thyroid pts ≥2 TSH tests/yr | 100% | ≥0.90 | Monitoring cadence |
| TSH within [0.001,150] | 100% | ≥1.0 | Assay-range integrity |
| Overt-hyper TSH suppressed (<0.1) | 100% | ≥0.95 | HPT-axis physiology |
| Hashimoto TPO-Ab positive | 100% | ≥0.85 | Autoimmune serology |
| Column count | 186 | ≥180 | Schema completeness (10 modules) |
Schema highlights by module (186 columns)
Demographics. Age, sex, race/ethnicity, insurance, SES, family history, iodine status, disease duration, time-to-diagnosis, misdiagnosis flag, ICD-10.
Disorder classification. Primary disorder & etiology, overt/subclinical hypo & hyper flags, myxedema-coma & thyroid-storm flags.
HPT-axis hormones. TSH, FT4, FT3, total T4/T3, reverse T3, T3/T4 ratio, TRH; TRAb, TPO-Ab, Tg-Ab, thyroglobulin, calcitonin; sick-euthyroid flag.
Hypothyroid symptoms. Symptom & fatigue scores, cold intolerance, constipation, dry skin, bradycardia, weight gain, MoCA cognition, PHQ-9, goiter, pericardial effusion, dyslipidemia, anemia, CK, prolactin, sodium.
Hyperthyroid symptoms. Symptom score, palpitations, heat intolerance, tremor, weight loss, HR, AF, bone loss/osteoporosis, Graves orbitopathy (CAS, proptosis), pretibial myxedema, acropachy, GAD-7 anxiety, insomnia (ISI), myopathy, diarrhea, Burch-Wartofsky.
Medication & treatment. Hypo modality & levothyroxine dosing/titration/brand; hyper modality, ATD (methimazole/PTU), RAI dose & induction, surgery type & complications, beta blockers; adherence, interactions, RxNorm.
Treatment response & QoL. Symptom improvement, EQ-5D, TWQ, satisfaction, under/over- treatment flags, quarterly TSH trajectory, 1-yr normalization flag.
Nodule & cancer. Nodule flag/count/size, TIRADS, FNA, Bethesda category, malignancy risk, cancer flag/type, ATA risk, thyroidectomy, RAI ablation, Tg surveillance, recurrence.
Comorbidities & labs. Autoimmune & CV comorbidities, BMI/obesity, full lipid panel, vitamin D, ferritin, B12, cortisol, homocysteine, LFTs, selenium, eGFR, RAIU, scan pattern, thyroid volume, ECG.
Utilization & pregnancy. Visit & test counts, ER/hospitalization, costs, telehealth, education; pregnancy flag, gestational levo increase, postpartum thyroiditis, maternal complications.
Coding standards. ICD-10, SNOMED, LOINC, RxNorm; FHIR R4 Observation bundle (full product).
Files
hc_end_004_sample.csv— 500-patient sample (186 columns)generate_sample_dataset_hc_end_004.py— reproducible generator + validation harnessvalidation_report.json/validation_report.md— full scorecardsweep_summary.json— 6-seed determinism results
Loading
import pandas as pd
df = pd.read_csv("hc_end_004_sample.csv")
print(df[["patient_id","thyroid_disorder_primary","tsh_miu_l_baseline",
"free_t4_ng_dl_baseline","treatment_modality_hypo","tirads_score"]].head())
from datasets import load_dataset
ds = load_dataset("csv", data_files="hc_end_004_sample.csv")
Use cases
- Thyroid-disorder classification from hormone panels (hypo/hyper/subclinical/autoimmune)
- Levothyroxine titration & TSH-normalization trajectory modeling
- Graves treatment-pathway and remission/relapse prediction
- Thyroid-nodule malignancy-risk modeling (TIRADS → Bethesda → ATA)
- Pregnancy thyroid-management and postpartum-thyroiditis tooling
- ML training where real thyroid EHR data is PHI-restricted
Honest limitations & disclosed generator behavior
This engine is among the better-calibrated XpertSystems SKUs; nonetheless, standard synthetic-data caveats and a few specifics apply:
- Independent symptom draws. Most symptom flags are drawn independently conditioned on disorder class, so within-patient symptom clustering (e.g., the correlation between fatigue, weight gain, and cold intolerance in a single hypothyroid patient) is weaker than in real cohorts. Disorder-level prevalences are correct.
- Quarterly TSH trajectory is monotonic-declining. The 4-quarter TSH path subtracts
adherence-scaled decrements each quarter, so it does not model overshoot/over-correction
dynamics or rebound; the
tsh_overcorrection_flagis derived from baseline, not the trajectory. - Cancer module prevalence is low (~3%). Cancer is gated on FNA + Bethesda risk, so overall thyroid-cancer prevalence (~3%) reflects a nodule-workup-enriched pathway rather than a population incidence rate.
- Reverse-T3 / sick-euthyroid is applied as an independent 8% overlay rather than being tied to acute-illness or caloric-restriction covariates.
General caveat: cross-field correlations beyond those explicitly modeled may be weaker than in real cohorts. Not for clinical decision-making — research/development use only.
Commercial product comparison
| Capability | This sample | Full HC-END-004 product |
|---|---|---|
| Patients | 500 | 20,000+ (configurable) |
| Seeds / cohorts | 1 | Multi-seed, reproducible |
| Formats | CSV | CSV + Parquet + JSON + FHIR R4 Bundle |
| Symptom clustering | Independent draws | Correlated within-patient symptom model |
| TSH trajectory | Monotonic 4-quarter | Full titration dynamics w/ overshoot |
| Cancer incidence | Workup-gated (~3%) | Tunable population-incidence mode |
| License | CC-BY-NC-4.0 | Commercial |
| Support & SLA | — | Included |
Full product, custom cohorts, or other endocrinology SKUs: pradeep@xpertsystems.ai
Citation
@dataset{xpertsystems_hc_end_004_2026,
title = {HC-END-004: Thyroid Disorders Synthetic Dataset},
author = {XpertSystems.ai},
year = {2026},
publisher = {XpertSystems.ai Synthetic Data Factory},
url = {https://xpertsystems.ai},
note = {Synthetic; CC-BY-NC-4.0 (sample). Calibrated to: NHANES III thyroid
prevalence (Hollowell et al. 2002, JCEM); Colorado Thyroid Disease
Prevalence Study (Canaris et al. 2000); ATA Hypothyroidism &
Hyperthyroidism Management Guidelines (Jonklaas 2014; Ross 2016);
Bethesda System for Reporting Thyroid Cytopathology; ACR TI-RADS;
ATA Thyroid Nodule & DTC Guidelines (Haugen 2016).}
}
Synthetic data generated by XpertSystems.ai. Not derived from real patient records. Not for clinical use.