All diseases

OMIM ID
249900
OMIM term:
METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY
Alternative terms:
METACHROMATIC LEUKODYSTROPHY DUE TO CEREBROSIDE SULFATASE ACTIVATOR DEFICIENCY
SAPOSIN B DEFICIENCY
(∗) Location:
10q22.1  
(†) Associated OMIM genes:
PSAP SAPOSIN A, INCLUDED; SAPA, INCLUDED  
(‡) Associated MGI genes:
Psap  

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* quick link - http://q.sanger.ac.uk/36apajcv