delayed cns myelination Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Delayed myelination in the central nervous system. (Human Phenotype Ontology, HP_0002188)
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9 genes associated with the delayed cns myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACY1 aminoacylase 1
BMP4 bone morphogenetic protein 4
D2HGDH D-2-hydroxyglutarate dehydrogenase
MUT methylmalonyl CoA mutase
PEX7 peroxisomal biogenesis factor 7
RBM8A RNA binding motif protein 8A
SHANK3 SH3 and multiple ankyrin repeat domains 3
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
UPB1 ureidopropionase, beta