Birk Barel mental retardation dysmorphism syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050675)
External Link http://www.omim.org/entry/612292
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Genes

1 genes associated with the Birk Barel mental retardation dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
KCNK9 potassium channel, two pore domain subfamily K, member 9