ivic syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/147750
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Genes

1 genes associated with the ivic syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SALL4 spalt-like transcription factor 4