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Summary Literature (4)
DOID:0060468 - Holt-Oram syndrome


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

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

In OMIM:
OMIM:142900 - HOLT-ORAM SYNDROME; HOS

In Mondo Disease Ontology:
MONDO:0007732 - Holt-Oram syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : tbx5

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant disease (is_a), syndrome (is_a)