neonatal death Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Death within the first 28 days of life. (Human Phenotype Ontology, HP_0003811)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003811
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Genes

14 genes associated with the neonatal death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DSP desmoplakin
ETFA electron-transfer-flavoprotein, alpha polypeptide
ETFB electron-transfer-flavoprotein, beta polypeptide
ETFDH electron-transferring-flavoprotein dehydrogenase
FAM20C family with sequence similarity 20, member C
FGFR3 fibroblast growth factor receptor 3
FLNB filamin B, beta
FOXF1 forkhead box F1
GLE1 GLE1 RNA export mediator
GLI3 GLI family zinc finger 3
HSPG2 heparan sulfate proteoglycan 2
LBR lamin B receptor
PIP5K1C phosphatidylinositol-4-phosphate 5-kinase, type I, gamma
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)