Informaţii despre
| Nume | | Other specified degenerative diseases of nervous system |
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| Pagina Web | | apps.who.int |
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Vezi şi
| Boli A-Z | | 2,4-Dienoyl-Coa Reductase Deficiency
Aicardi-Goutieres Syndrome
Autosomal Recessive Cerebral Atrophy
Combined Oxidative Phosphorylation Deficiency 11
Combined Oxidative Phosphorylation Deficiency 15
Combined Oxidative Phosphorylation Deficiency 20
Combined Oxidative Phosphorylation Deficiency 6
Combined Oxidative Phosphorylation Deficiency 7
Encephalopathy, Acute, Infection-Induced 4
Encephalopathy Due to Defective Mitochondrial and Peroxisomal Fission 1
Encephalopathy, Ethylmalonic
Encephalopathy, Familial, with Neuroserpin Inclusion Bodies
Encephalopathy, Progressive, with or Without Lipodystrophy
Epileptic Encephalopathy, Early Infantile, 39
Leigh Syndrome
Leigh Syndrome, French Canadian Type
Leigh Syndrome with Leukodystrophy
Leigh Syndrome with Nephrotic Syndrome
Mitochondrial Dna Depletion Syndrome 4a
Mitochondrial Dna Depletion Syndrome 8a
Multiple Mitochondrial Dysfunctions Syndrome 3
Neurodegeneration Due to Cerebral Folate Transport Deficiency
Neuropathy, Ataxia, and Retinitis Pigmentosa
Peho Syndrome
Prkar1b-Related Neurodegenerative Dementia with Intermediate Filaments
Spastic Paraplegia 79, Autosomal Recessive
Syndromic Sensorineural Deafness Due to Combined Oxidative Phosphorylation Defect
X-Linked Intellectual Disability-Ataxia-Apraxia Syndrome
X-Linked Neurodegenerative Syndrome, Bertini Type
X-Linked Neurodegenerative Syndrome, Hamel Type |
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