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ORPHA:2312

Transient familial neonatal hyperbilirubinemia

high confidenceDisorder

Also known as: Lucey-Driscoll syndrome

Query health: suspect — Only one of 2 strategies returned hits (phrase).

Publications

28

36.4th percentile

Trials

0

Interventional, condition-specific

Researchers

144

Distinct authors in sample

Gene link

—

Readiness

2/6

Stages with a signal

Clinical definition (Orphanet)

A rare genetic hepatic disease characterized by very high serum bilirubin levels in a newborn, clinically presenting as jaundice during the first few days of life. The condition is usually self-resolving, although in some cases it can lead to kernicterus with corresponding symptoms (including lethargy, high-pitched crying, , missing reflexes, vomiting, or , among others), which may result in chronic disability and even death.

How rare: Not yet documented

Orphanet entry

Cross-references

Joined from Mondo / Orphanet. MeSH labels may enter searches; UMLS / OMIM / NCIT are stored for reference.

Additional Mondo synonyms (1)

hyperbilirubinemia, familial transient neonatal

Research stages

Trial readiness signals

Where this condition sits on an open-data research pipeline — not how close a treatment is, and not medical advice. Empty stages often mean “not in these databases under this Mondo ID,” not “impossible.”

2/6 stages with a signal

No specific-condition interventional trial, but broader-category trials exist — discuss eligibility with a clinician.

  1. Gene identifiedNot found

    No GenCC disease–gene assertion in this build

  2. LiteraturePresent

    28 matched papers (19 in last 10 years) Source

  3. Phenotype characterisedNot checked

    Not yet enriched from Monarch / HPO

  4. Animal modelNot checked

    Not yet enriched from Monarch / Alliance

  5. Orphan designationNot checked

    FDA/EMA orphan-drug designation not enriched yet

  6. Interventional trialPartial

    None under the specific name; 90 for broader category hyperbilirubinemia

Biology

Genes and phenotypes

Gene–disease validity from GenCC, plus phenotypes and animal models joined from Monarch Initiative via Mondo ID — not a clinical diagnosis aid.

Do we know what causes it?

Not yet — the cause hasn't been pinned down in GenCC.

No strong gene–disease assertion joined for this Orphanet entity.

Phenotypes (Monarch / HPO)

Not enriched in this build — Monarch phenotype joins were not run for this record.

Animal models (Monarch / Alliance)

Not enriched in this build.

Literature

Is anyone studying this?

28

28 papers have ever been published on this condition (under this name). For scale, breast cancer has over 700,000. Median papers in the last 10 years for a rare disease in this dataset (publications denominator n=5449) is 41.

28 papers since the earliest indexed year in this search — median last-10-year count for a rare disease in this dataset is 41 (publications denominator n=5449).

19 in the last 10 years · high confidence · 36.4th percentile (publications denominator)

Phrase hits: 28 · MeSH hits: 0

Open Europe PMC search

Who's working on it?

144

Distinct author names in 28 sampled papers — named people below.

Who's working on it?

No interventional trial matched this name; these authors publish on it in the sampled literature — a practical starting point for contact.

  1. 01
    Liu Y3 papers · 2026

    Department of Genetics, Jiangxi Maternal and Child Health Hospital, 330006, Nanchang, China.

    Papers in Europe PMC
  2. 02
    ARIAS IM2 papers · 1965
    Papers in Europe PMC
  3. 03
    Huang H2 papers · 2025

    BGI Genomics, BGI-Shenzhen, 518083, Shenzhen, China.

    Papers in Europe PMC
  4. 04
    Wang X2 papers · 2024

    People's Hospital of Ningxia Hui Autonomous Region (Ningxia Medical University), Ningxia Eye Hospital, Yinchuan, 750001, China.

    Papers in Europe PMC
  5. 05
    Xiao R2 papers · 2026

    Biosan (Hangzhou) Clinical Laboratory, Hangzhou, 310000, China.

    Papers in Europe PMC
  6. 06
    Zhang Y2 papers · 2024

    Department of Neonatology, Tianjin Children's Hospital/Tianjin University Children's Hospital, Beichen District, Tianjin, China.

    Papers in Europe PMC
  7. 07
    Abuduxikuer K1 paper · 2018

    Department of Hepatology, Children's Hospital of Fudan University.

    Papers in Europe PMC
  8. 08
    Al-Zamil M1 paper · 2023

    Department of Physiotherapy, Faculty of Continuing Medical Education, Peoples' Friendship University of Russia, 11798 Moscow, Russia.

    Papers in Europe PMC
  9. 09
    Aleksunes LM1 paper · 2016

    Department of Pharmacology and Toxicology, Rutgers University, Piscataway, New Jersey.

    Papers in Europe PMC
  10. 10
    Altynbekov KS1 paper · 2023

    Republican Scientific and Practical Center of Mental Health, Almaty 050022, Kazakhstan.

    Papers in Europe PMC

Clinical research

Is a treatment being tested?

0

interventional trials for this specific condition

No interventional trial testing a treatment matched this specific condition name on ClinicalTrials.gov (observational studies and pan-disease registries are listed separately when present). 90 trials are registered for hyperbilirubinemia, the broader category — shown separately because they may or may not enrol this specific subtype.

Data as of 27 July 2026

No matched interventional trials. This is true for 73% of diseases in the trials denominator (5114 of 7003). Here are the researchers publishing on it.

high confidence · 36.5th percentile (trials denominator)

Recruiting interventional trials

From the matched ClinicalTrials.gov set

No interventional trial testing a treatment was found for this specific condition name on ClinicalTrials.gov.

90 interventional trials matched hyperbilirubinemia, the broader category — listed below. Those studies are not counted in the condition-specific total.

Broader category: hyperbilirubinemia

90

Interventional trials for the parent category, exclusive of NCT IDs already counted above. Eligibility for this subtype is not guaranteed.

Worth raising with a clinician. How we count trials.

Recruiting under the broader category

Where to find support

We do not yet link condition-specific patient organisations. These umbrella groups support undiagnosed and ultra-rare families:

India — NPRD

Last verified 2026-07-26

This ORPHAcode is not on our curated NPRD list (direct or Mondo-parent match). That does not decide clinical eligibility; families in India should ask a notified Centre of Excellence about current coverage.

Hand-curated for this project. ORPHAcode mappings are best-effort and may be incomplete or imprecise for umbrella categories. Parent (Mondo) matches mean the policy lists a broader category — confirm eligibility with a Centre of Excellence. Financial entitlements summarised from public policy statements and may change. This is not official government guidance.

How we counted this

Europe PMC query (preferred label + any corrected label + Orphanet and Mondo exact synonyms, stoplisted; unioned with resolved MeSH labels when available). UMLS / OMIM / NCIT cross-references are stored on the overview but are not added to the query string.

"Transient familial neonatal hyperbilirubinemia" OR "Lucey-Driscoll syndrome" OR "hyperbilirubinemia, familial transient neonatal"

Run this search on Europe PMC

ClinicalTrials.gov query (quoted phrases + MeSH via query.cond, plus recall-expansion terms when used):

"Transient familial neonatal hyperbilirubinemia" OR "Lucey-Driscoll syndrome" OR "hyperbilirubinemia, familial transient neonatal" OR "hereditary hyperbilirubinemia"

Recall-expansion terms: hereditary hyperbilirubinemia

Study-type breakdown: 0 interventional · 0 observational · 0 expanded access. Only interventional studies enter the trial headline.

Parent-category trials query:

"hyperbilirubinemia"

Query health: suspect — strategies attempted: phrase, recall-expansion; with hits: phrase

Run this search on ClinicalTrials.gov

Confidence reasoning

  • Preferred label is multi-word and distinctive
  • No synonyms dropped by stoplist
  • No label/synonym collisions with other diseases in this corpus

Ingested 2026-07-26T19:48:00.618Z