All diseases

OMIM ID
218000
OMIM term:
AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN
Alternative terms:
CHARLEVOIX DISEASE
ANDERMANN SYNDROME
POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUS CALLOSUM
CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY
(∗) Location:
15q14  
(†) Associated OMIM genes:
SLC12A6  
(‡) Associated MGI genes:
Slc12a6  

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* quick link - http://q.sanger.ac.uk/hnv38lg9