ORPHA:583602
Neu-Laxova syndrome due to phosphoserine aminotransferase deficiency
Also known as: Phosphoserine aminotransferase deficiency, prenatal form
Query health: suspect — Only one of 2 strategies returned hits (phrase).
Publications
11
28.7th percentile
Trials
0
Interventional, condition-specific
Researchers
90
Distinct authors in sample
Gene link
PSAT1
Strong
Readiness
2/6
Stages with a signal
Cross-references
Joined from Mondo / Orphanet. MeSH labels may enter searches; UMLS / OMIM / NCIT are stored for reference.
- MONDO:0014466
- OMIM:616038
- UMLS:C4015019
Additional Mondo synonyms (5)
Neu-Laxova syndrome 2 · Neu-Laxova syndrome caused by mutation in PSAT1 · Neu-Laxova syndrome type 2 · PSAT1 Neu-Laxova syndrome · phosphoserine aminotransferase deficiency, prenatal form
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 matched interventional trial; the gene is known and literature exists — preclinical or natural-history work may still be the practical next step.
- Gene identifiedPresent
Strong — PSAT1
- LiteraturePresent
11 matched papers (11 in last 10 years) Source
- Phenotype characterisedNot checked
Not yet enriched from Monarch / HPO
- Animal modelNot checked
Not yet enriched from Monarch / Alliance
- Orphan designationNot checked
FDA/EMA orphan-drug designation not enriched yet
- Interventional trialNot found
No matched interventional trial under our ClinicalTrials.gov rules
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?
Yes — we know a specific gene responsible (PSAT1).
GenCC classification: Strong.
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?
11
11 papers have ever been indexed 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.
11 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).
11 in the last 10 years · high confidence · 28.7th percentile (publications denominator)
Phrase hits: 11 · MeSH hits: 0
Who's working on it?
90
Distinct author names in 11 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.
- 01Cromie GA2 papers · 2023
Pacific Northwest Research Institute, Seattle, Washington.
Papers in Europe PMC - 02Dudley AM2 papers · 2023
Pacific Northwest Research Institute, Seattle, Washington.
Papers in Europe PMC - 03
- 04Ascari G1 paper · 2021
Center for Medical Genetics Ghent, Ghent University Hospital, Ghent, Belgium.
Papers in Europe PMC - 05Ashmead J1 paper · 2020
Pacific Northwest Research Institute, Seattle, Washington.
Papers in Europe PMC - 06Bauwens M1 paper · 2021
Center for Medical Genetics Ghent, Ghent University Hospital, Ghent, Belgium.
Papers in Europe PMC - 07Bertelsen M1 paper · 2021
The Kennedy Center, Department of Clinical Genetics, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Papers in Europe PMC - 08Bettati S1 paper · 2023
Department of Medicine and Surgery, University of Parma, 43124 Parma, Italy.
Papers in Europe PMC - 09Bianchera A1 paper · 2023
Department of Food and Drug, University of Parma, 43124 Parma, Italy.
Papers in Europe PMC - 10Bruno S1 paper · 2023
Department of Food and Drug, University of Parma, 43124 Parma, Italy.
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).
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.
Broader category Neu-Laxova syndrome also has no matched interventional trial. See who's working on it — people publishing on this disease are often the practical next contact when no trial is listed.
Broader category: Neu-Laxova syndrome
0
Interventional trials for the parent category, exclusive of NCT IDs already counted above. Eligibility for this subtype is not guaranteed.
Parent-category matching found a broader label but no interventional trials under it. How we count trials.
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 2026-07-26This 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.
"Neu-Laxova syndrome due to phosphoserine aminotransferase deficiency" OR "Phosphoserine aminotransferase deficiency, prenatal form" OR "Neu-Laxova syndrome 2" OR "Neu-Laxova syndrome caused by mutation in PSAT1" OR "Neu-Laxova syndrome type 2" OR "PSAT1 Neu-Laxova syndrome"
ClinicalTrials.gov query (quoted phrases + MeSH via query.cond, plus recall-expansion terms when used):
"Neu-Laxova syndrome due to phosphoserine aminotransferase deficiency" OR "Phosphoserine aminotransferase deficiency, prenatal form" OR "Neu-Laxova syndrome 2" OR "Neu-Laxova syndrome caused by mutation in PSAT1" OR "Neu-Laxova syndrome type 2" OR "PSAT1 Neu-Laxova syndrome" OR "PSAT1"
Recall-expansion terms: PSAT1
Study-type breakdown: 0 interventional · 0 observational · 0 expanded access. Only interventional studies enter the trial headline.
Parent-category trials query:
"Neu-Laxova syndrome"
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 2026-07-27T18:42:44.791Z