Hydrops Fetalis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description The abnormal accumulation of fluid in two or more fetal compartments, including ascites, pleural effusion, pericardial effusion, and skin edema. (Human Phenotype Ontology, HP_0001789)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D015160
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Genes

1 genes/proteins associated with the disease Hydrops Fetalis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CCBE1 collagen and calcium binding EGF domains 1 2.88009