All diseases

OMIM ID
226750
OMIM term:
KOHLSCHUTTER-TONZ SYNDROME; KTZS
Alternative terms:
EPILEPSY AND YELLOW TEETH
EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA
KOHLSCHUTTER SYNDROME
(∗) Location:
16p13.3  
(†) Associated OMIM genes:
ROGDI  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/xc0kmco2