|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A syndrome that is characterized by advanced bone age, failure to thrive, respiratory problems, dysmorphic facial features, and variable mental retardation. (Human Disease Ontology, DOID_0050858)|
|Downloads & Tools|
1 genes associated with the marshall-smith syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
|NFIX||nuclear factor I/X (CCAAT-binding transcription factor)|