Alpers syndrome
|
(Orphanet:726)
|
Combined oxidative phosphorylation defect type 11
|
(Orphanet:324535)
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17
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(OMIM:615473)
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Early infantile epileptic encephalopathy without suppression burst
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(Orphanet:369894)
|
Guanidinoacetate methyltransferase deficiency
|
(Orphanet:382)
|
Infantile epileptic-dyskinetic encephalopathy
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(Orphanet:364063)
|
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4
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(OMIM:615228)
|
Methylmalonic acidemia with homocystinuria, type cblX
|
(Orphanet:369962)
|
Phosphoserine aminotransferase deficiency
|
(Orphanet:284417)
|
Spasticity - intellectual deficit - X-linked epilepsy
|
(Orphanet:3175)
|
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A
|
(Orphanet:308386)
|
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B
|
(Orphanet:308393)
|