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Disease

Jackson-Weiss syndrome

Also known as JWS, craniosynostosis-midfacial hypoplasia-foot abnormalities syndrome, craniosynostosis, midfacial hypoplasia, and foot abnormalities.

3
Associated genes
2
Related proteins

What's happening now

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

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Associated genes

3 matches

Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.

FGFR20.81FGFR10.72SOX20.52

Disease biology

2 matches

Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.

Fibroblast growth factor receptor 2via FGFR20.81Fibroblast growth factor receptor 1via FGFR10.72

Reference

Authoritative identity, definition & identifiers.

Synonyms

JWS, craniosynostosis-midfacial hypoplasia-foot abnormalities syndrome, craniosynostosis, midfacial hypoplasia, and foot abnormalities

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.