|
 AUTOSOMAL DOMINANT, 1
|
AUTOSOMAL RECESSIVE
|
LEIGH SYNDROME (LS)
|
MITOCHOND
|
MITOCHONDRIAL DNA DEPLETION
|
MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)
|
MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (MTDPS4A)
|
MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE)
|
MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE), INCLUDED
|
MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MTDPS4B)
|
PROGRESSIVE EXTERNAL OPHTHA
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETI
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS AUTOSOMAL RECESSIVE (PEOB)
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT, 1 (PEOA1)
|
SENSORY ATAXIC NEUROPATHY DYSARTHRIA AND OPHTHALMOPARESIS (SANDO)
|
SENSORY ATAXIC NEUROPATHY,
|
SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS
|
SPINOCEREBELLAR ATAXIA WITH EPILEPSY
|
SPINOCEREBELLAR ATAXIA WITH EPILEPSY, INCLUDED;;
|
POLG
5428
84
9
22
2
69
