| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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) |
| External Link | http://www.omim.org/entry/602535 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the marshall-smith syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| NFIX | nuclear factor I/X (CCAAT-binding transcription factor) |
