|OBO ID: DOID:0060468|
|Term Name:||Holt-Oram syndrome||Search Ontology:|
|Definition:||A syndrome characterized by congenital anomalies located_in heart and located_in upper limb. (4)|
|Ontology:||Human Disease (DOID:0060468)|
|is a type of:||
OTHER Holt-Oram syndrome PAGES
PHENOTYPE No data available
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