abnormal ciliary ganglion morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the parasympathetic ganglia in the orbit behind the eye that receives preganglionic innervation through the oculomotor nerve (Mammalian Phenotype Ontology, MP_0004990)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004990
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3 gene mutations causing the abnormal ciliary ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
NRTN neurturin
OTX2 orthodenticle homeobox 2
PHOX2B paired-like homeobox 2b