All diseases

OMIM ID
609528
OMIM term:
CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMA SYNDROME
Alternative terms:

(∗) Location:
22q11.21  
(†) Associated OMIM genes:
SNAP29  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/ylvp0yqj