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Disease

Abnormalities, Multiple

Late-stage therapeutic developmentEmerging research
1
Publications
1
Clinical trials
2023
Latest publication
Latest activity
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Recent clinical, regulatory, research and industry developments relating to this disease.

The impact of SETBP1 mutations in neurological diseases and cancer.

Research2023-07-25Genes to cells : devoted to molecular & cellular mechanisms

What's happening now

An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.

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Clinical trials

1 sponsors · 0 new · 0 completed in the last 12 months (net +0)

The current development programme across all trial phases.

Research activity

1 papers

Key research shaping understanding of this disease, combining the latest publications with the most influential evidence.

Most influential

The impact of SETBP1 mutations in neurological diseases and cancer.

Genes to cells : devoted to molecular & cellular mechanisms · 2023 · 10 cites
Recent publications

The impact of SETBP1 mutations in neurological diseases and cancer.

Genes to cells : devoted to molecular & cellular mechanisms · 2023 · 10 cites
Major themes4
  • Abnormalities, Multiple1
  • Craniofacial Abnormalities1
  • Intellectual Disability1
  • Neoplasms1
Leading journals1
  • Genes to cells : devoted to molecular & cellular mechanisms1
Leading researchers2
  • Kohyanagi N1
  • Ohama T1
Affiliations (unnormalised)1
  • Laboratory of Veterinary Pharmacology1

Reference

Authoritative identity, definition & identifiers.

Defined in MeSH

Congenital abnormalities that affect more than one organ or body structure.

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
  • Research activity — Europe PMC (EMBL-EBI) + OpenAlex-derived paper links
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.