Holt-Oram syndrome

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Summary

Literature (6)

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,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: tbx5

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0007732 - Holt-Oram syndrome

MONDO:0007732 - Holt-Oram syndrome

OMIM:

OMIM:142900 - HOLT-ORAM SYNDROME; HOS

OMIM:142900 - HOLT-ORAM SYNDROME; HOS

Other Model Organisms: AGR, 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)