All diseases

OMIM ID
147750
OMIM term:
IVIC SYNDROME
Alternative terms:
RADIAL RAY DEFECTS, HEARING IMPAIRMENT, EXTERNAL OPHTHALMOPLEGIA, AND THROMBOCYTOPENIA
OCULOOTORADIAL SYNDROME; OORS
(∗) Location:
20q13.2  
(†) Associated OMIM genes:
SALL4  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/3ffuasa1