All diseases

OMIM ID
220500
OMIM term:
DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, AND MENTAL RETARDATION SYNDROME
Alternative terms:
DOOR SYNDROME
DIGITORENOCEREBRAL SYNDROME
DRC SYNDROME
BRACHYDACTYLY DUE TO ABSENCE OF DISTAL PHALANGES
ERONEN SYNDROME
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/ysjj45d4