failure to thrive in infancy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001531
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Genes

10 genes associated with the failure to thrive in infancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COG1 component of oligomeric golgi complex 1
CTNS cystinosin, lysosomal cystine transporter
DYRK1A dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
ERCC1 excision repair cross-complementation group 1
LTC4S leukotriene C4 synthase
MAGEL2 melanoma antigen family L2
NDN necdin, melanoma antigen (MAGE) family member
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RET ret proto-oncogene
SNRPN small nuclear ribonucleoprotein polypeptide N