|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||IVIC syndrome is a very rare genetic malformation syndrome characterized by upper limb anomalies (radial ray defects, carpal bone fusion), extraocular motor disturbances, and congenital bilateral non-progressive mixed hearing loss. (Orphanet Rare Disease Ontology, Orphanet_2307)|
|Downloads & Tools|
1 genes associated with the ivic syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
|SALL4||spalt-like transcription factor 4|