Arnold-Chiari Malformation Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Arnold-Chiari malformation consists of a downward displacement of the cerebellar tonsils and the medulla through the foramen magnum, sometimes causing hydrocephalus as a result of obstruction of CSF outflow. (Human Phenotype Ontology, HP_0002308)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D001139
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Genes

4 genes/proteins associated with the disease Arnold-Chiari Malformation from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ERF Ets2 repressor factor 2.88009
PAX3 paired box 3 1.15458
RARG retinoic acid receptor, gamma 1.0869
TGFB3 transforming growth factor, beta 3 1.02299