All diseases

OMIM ID
249620
OMIM term:
OHDO SYNDROME
Alternative terms:
OHDO BLEPHAROPHIMOSIS SYNDROME
MENTAL RETARDATION, CONGENITAL HEART DISEASE, BLEPHAROPHIMOSIS, BLEPHAROPTOSIS, AND HYPOPLASTIC TEETH
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/o621cl1s