All diseases

OMIM ID
301500
OMIM term:
FABRY DISEASE
Alternative terms:
ANGIOKERATOMA CORPORIS DIFFUSUM
ANDERSON-FABRY DISEASE
HEREDITARY DYSTOPIC LIPIDOSIS
ALPHA-GALACTOSIDASE A DEFICIENCY
GLA DEFICIENCY
CERAMIDE TRIHEXOSIDASE DEFICIENCY FABRY DISEASE, CARDIAC VARIANT, INCLUDED
(∗) Location:
Xq22.1  
(†) Associated OMIM genes:
GLA  
(‡) Associated MGI genes:
Gla  

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