Condition: Nasogastric tube feeding in infancy


rs867410737 in ATP5F1D gene and Nasogastric tube feeding in infancy PMID 29478781 2018 Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.

rs864309486 in GMNN gene and Nasogastric tube feeding in infancy PMID 26637980 2015 De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.