Craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies

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Subtype of: Craniosynostosis
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies
MONDO_0013740
CYP26B1 Unknown
22019272 27410456
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies.
5 View disease cluster →
Lethal occipital encephalocele-skeletal dysplasia syndrome 1 shared geneCYP26B1 Related via 1 shared gene including CYP26B1. Mouth disease 1 shared geneCYP26B1 Related via 1 shared gene including CYP26B1. Craniosynostosis 1 shared geneCYP26B1 Related via 1 shared gene including CYP26B1. Colorectal adenoma 1 shared geneCYP26B1 Related via 1 shared gene including CYP26B1. Desbuquois syndrome 1 shared geneCYP26B1 Related via 1 shared gene including CYP26B1.