Term: Radiohumeral Fusions with Other Skeletal and Craniofacial Anomalies;
OMIM ID: 614416

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene	Human Gene		Characteristics of this human disease are associated with mutations in...
Cyp26b1 CYP26B1			...the human gene.      MGI data currently do not associate this disease with mutations in the orthologous mouse gene.