marshall-smith syndrome Gene Set

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
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Genes

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)