All diseases

OMIM ID
252011
OMIM term:
MITOCHONDRIAL COMPLEX II DEFICIENCY
Alternative terms:

(∗) Location:
19q13.12   5p15.33  
(†) Associated OMIM genes:
SDHA   SDHAF1  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/qrfwjomi