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heart-hand syndrome, Slovenian type

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description A rare autosomal dominant form of heart-hand syndrome, first described in members of a Slovenian family, that is characterized by adult onset, progressive cardiac conduction disease, tachyarrhythmias that can lead to sudden death, dilated cardiomyopathy and brachydactyly, with the hands less severely affected than the feet. Muscle weakness and/or myopathic electromyographic findings have been observed in some cases.
Uniprot Description Heart-hand syndrome (HHS) is a clinically and genetically heterogeneous disorder characterized by the co-occurrence of a congenital cardiac disease and limb malformations.
Mondo Term and Equivalent IDs
MONDO:0012417:  heart-hand syndrome, Slovenian type
GARD:0009846: 
MESH:C535852: 
Orphanet:168796: 
SCTID:721014007: 
UMLS:C1857829: