mild postnatal growth retardation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A mild degree of slow or limited growth after birth, being between two and three standard deviations below age- and sex-related norms. (Human Phenotype Ontology, HP_0001530)
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3 genes associated with the mild postnatal growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CCBE1 collagen and calcium binding EGF domains 1
CDAN1 codanin 1
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha