- OMIM ID
-
601088
- OMIM term:
- CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKE FACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION
- Alternative terms:
-
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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