All diseases

OMIM ID
242500
OMIM term:
ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE
Alternative terms:
HARLEQUIN ICHTHYOSIS
'HARLEQUIN FETUS'
(∗) Location:
2q35  
(†) Associated OMIM genes:
ABCA12  
(‡) Associated MGI genes:
Abca12   Cst6  

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* quick link - http://q.sanger.ac.uk/g471afty