|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A type of autosomal dominant inheritance involving a gene that is imprinted with maternal silencing. (Human Phenotype Ontology, HP_0012275)|
|Downloads & Tools|
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.
|KANK1||KN motif and ankyrin repeat domains 1|