autosomal dominant inheritance with maternal imprinting Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of autosomal dominant inheritance involving a gene that is imprinted with maternal silencing. (Human Phenotype Ontology, HP_0012275)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012275
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Genes

1 genes associated with the autosomal dominant inheritance with maternal imprinting phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
KANK1 KN motif and ankyrin repeat domains 1