|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An autosomal recessive disorder characterized by severe intrauterine and postnatal growth retardation, microcephaly, bilateral microtia and hypoplastic patellae. (Human Disease Ontology, DOID_0060306)|
|Downloads & Tools|
5 genes/proteins associated with the disease Meier-Gorlin syndrome from the curated CTD Gene-Disease Associations dataset.