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IVIC syndrome

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo 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.
Uniprot Description Autosomal dominant condition characterized by upper limbs anomalies (radial ray defects, carpal bones fusion), extraocular motor disturbances, congenital bilateral non-progressive mixed hearing loss. Other less consistent malformations include heart involvement, mild thrombocytopenia and leukocytosis (before age 50), shoulder girdle hypoplasia, imperforate anus, kidney malrotation or rectovaginal fistula. The IVIC syndrome is an allelic disorder of Duane-radial ray syndrome (DRRS) with a similar phenotype.
Mondo Term and Equivalent IDs
MONDO:0007836:  IVIC syndrome
DOID:0111381: 
GARD:0000269: 
MESH:C535544: 
Orphanet:2307: 
SCTID:722019000: 
UMLS:C1327918: