All diseases

OMIM ID
245010
OMIM term:
HAIM-MUNK SYNDROME; HMS
Alternative terms:
KERATOSIS PALMOPLANTARIS WITH PERIODONTOPATHIA AND ONYCHOGRYPOSIS
COCHIN JEWISH DISORDER
(∗) Location:
11q14.2  
(†) Associated OMIM genes:
CTSC  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/torzg7pg