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Holt-Oram syndrome
What is Holt-Oram syndrome?
A genetic syndrome with limb reduction defects characterized by skeletal abnormalities of the upper limbs and mild-to-severe congenital cardiac defects.
Other condition names
Atriodigital dysplasia type 1
HOS
Heart-hand syndrome type 1
Inheritance type
Autosomal dominant
Age of Onset
Neonatal
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on
"https://www.orphadata.com"
. Data version 1.3.16 / 4.1.7.