|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050675)|
|Downloads & Tools|
1 genes/proteins associated with the disease Birk-Barel Mental Retardation Dysmorphism Syndrome from the curated CTD Gene-Disease Associations dataset.
|KCNK9||potassium channel, two pore domain subfamily K, member 9||2.88009|