Hydrocephalus, X-linked Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A cerebral degeneration characterized by an abnormal accumulation of cerebrospinal fluid in the ventricles of the brain, leading to progressive enlargement of the head. (Human Disease Ontology, DOID_10908)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536078
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Genes

1 genes/proteins associated with the disease Hydrocephalus, X-linked from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
L1CAM L1 cell adhesion molecule 2.88009