All diseases

OMIM ID
612949
OMIM term:
HYPOMYELINATION, GLOBAL CEREBRAL
Alternative terms:
ASPARTATE-GLUTAMATE CARRIER 1 DEFICIENCY
AGC1 DEFICIENCY
(∗) Location:
2q31.1  
(†) Associated OMIM genes:
SLC25A12  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/21bejwy4