All diseases

OMIM ID
228000
OMIM term:
FARBER LIPOGRANULOMATOSIS
Alternative terms:
FARBER DISEASE
CERAMIDASE DEFICIENCY
ACID CERAMIDASE DEFICIENCY
AC DEFICIENCY
N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY
(∗) Location:
8p22  
(†) Associated OMIM genes:
ASAH1  
(‡) Associated MGI genes:
Asah1  

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* quick link - http://q.sanger.ac.uk/1ghu4cox