|
seizures, familial febrile, 4
|
C565788 |
|
|
congenital deafness, macular dystrophy, and psychiatric disorders myoclonic epilepsy
|
C565786 |
|
|
cytochrome c oxidase deficiency, fatal infantile, with cardioencephalomyopathy
|
C565784 |
|
|
mitochondrial oxidative phosphorylation disorder due to nDNA anomalies
|
16578 |
|
|
mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies
|
16578 |
|
|
advanced sleep-phase syndrome, familial
|
C565789 |
|
|
partial, with variable foci epilepsy
|
C565785 |
|
|
fatal infantile, with cardioencephalomyopathy cytochrome c oxidase deficiency
|
C565784 |
|
