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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
Echinobase Genes

MIM:142900 - holt-oram syndrome; hos |
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)