|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050675)|
|Downloads & Tools|
1 genes associated with the Birk Barel mental retardation dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|KCNK9||potassium channel, two pore domain subfamily K, member 9|