All diseases

OMIM ID
142900
OMIM term:
HOLT-ORAM SYNDROME; HOS
Alternative terms:
HOS1
HEART-HAND SYNDROME
ATRIODIGITAL DYSPLASIA
(∗) Location:
12q24.21  
(†) Associated OMIM genes:
TBX5  
(‡) Associated MGI genes:
Tbx5   vsd  

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* quick link - http://q.sanger.ac.uk/h6ul21tr