Oculootoradial syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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://ctdbase.org/detail.go?type=disease&acc=MESH:C535544
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Genes

1 genes/proteins associated with the disease Oculootoradial syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SALL4 spalt-like transcription factor 4 2.88009