All diseases

OMIM ID
603041
OMIM term:
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1
Alternative terms:
MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME, TYMP-RELATED
MNGIE, TYMP-RELATED
MYONEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME
POLYNEUROPATHY, OPHTHALMOPLEGIA, LEUKOENCEPHALOPATHY, AND INTESTINAL PSEUDOOBSTRUCTION
POLIP SYNDROME
(∗) Location:
22q13.33  
(†) Associated OMIM genes:
TYMP  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/ux4xmnua