All diseases

OMIM ID
256550
OMIM term:
NEURAMINIDASE DEFICIENCY
Alternative terms:
SIALIDOSIS, TYPE II
MUCOLIPIDOSIS I
ML I
LIPOMUCOPOLYSACCHARIDOSIS
SIALIDASE DEFICIENCY
GLYCOPROTEIN NEURAMINIDASE DEFICIENCY
NEUG DEFICIENCY
NEURAMINIDASE 1 DEFICIENCY
NEU DEFICIENCY
NEU1 DEFICIENCY SIALIDOSIS, TYPE I, INCLUDED
CHERRY RED SPOT--MYOCLONUS SYNDROME, INCLUDED
MYOCLONUS--CHERRY RED SPOT SYNDROME, INCLUDED
(∗) Location:
6p21.33  
(†) Associated OMIM genes:
NEU1  
(‡) Associated MGI genes:
Neu1  

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* quick link - http://q.sanger.ac.uk/19a16kl1