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.