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2 entries on 1 page. Showing entries 1 - 2.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00390 308930 Leigh syndrome, X-linked, 308930 (3) 308930 0 0 PDHA1 - -
00442 PDHAD PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD 312170 0 0 , PDHA1 - -