severe intrauterine growth retardation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Intrauterine growth retardation that is 4 or more standard deviations below average, corrected for sex and gestational age. (Human Phenotype Ontology, HP_0008846)
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2 genes associated with the severe intrauterine growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
TBCE tubulin folding cofactor E