severe postnatal growth retardation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Severely slow or limited growth after birth, being four standard deviations or more below age- and sex-related norms. (Human Phenotype Ontology, HP_0008850)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008850
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Genes

6 genes associated with the severe postnatal growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ERCC8 excision repair cross-complementation group 8
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
LHX4 LIM homeobox 4
POU1F1 POU class 1 homeobox 1
TBC1D20 TBC1 domain family, member 20
TSHB thyroid stimulating hormone, beta