All diseases

OMIM ID
234500
OMIM term:
HARTNUP DISORDER
Alternative terms:
HND
HARTNUP DISEASE
(∗) Location:
5p15.33  
(†) Associated OMIM genes:
SLC6A19  
(‡) Associated MGI genes:
Slc6a19  

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* quick link - http://q.sanger.ac.uk/2kelbyzw