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Summary Literature (0)
DOID:0060468 - Holt-Oram syndrome

Disease Ontology Definition:A syndrome characterized by congenital anomalies located_in heart and located_in upper limb.

Synonyms: atriodigital dysplasia, atrio-digital syndrome, heart-hand syndrome

Xenbase Genes : tbx5

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007732 - Holt-Oram syndrome


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), syndrome (is_a)