All diseases

OMIM ID
251270
OMIM term:
MICROCEPHALY AND CHORIORETINOPATHY WITH OR WITHOUT MENTAL RETARDATION, AUTOSOMAL RECESSIVE
Alternative terms:

(∗) Location:
22q13.33  
(†) Associated OMIM genes:
TUBGCP6  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/vwnjytmm