All diseases

OMIM ID
607483
OMIM term:
THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2
Alternative terms:
BASAL GANGLIA DISEASE, BIOTIN-RESPONSIVE; BBGD
ENCEPHALOPATHY, THIAMINE-RESPONSIVE
(∗) Location:
2q36.3  
(†) Associated OMIM genes:
SLC19A3  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/bfq3r48z