All diseases

OMIM ID
181600
OMIM term:
SCLEROTYLOSIS
Alternative terms:
TYS
SCLEROATROPHIC AND KERATOTIC DERMATOSIS OF LIMBS
HURIEZ SYNDROME; HRZ
(∗) Location:
4q23  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/kw20wvaw