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ȘTIINȚE APLICATE
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Boli, Tulburări & Simptome
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XX Boli-semne, simptome
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Mitochondrial Metabolism Disease
Informaţii despre
Nume
Mitochondrial Metabolism Disease
Pagina Web
www.malacards.org
Clasificare globală Malacards
Boli metabolice
Vezi şi
Boli A-Z
3-Hydroxyacyl-Coa Dehydrogenase Deficiency
3-Methylglutaconic Aciduria, Type Iii
3-Methylglutaconic Aciduria, Type Iv
3-Methylglutaconic Aciduria, Type V
Acute Liver Failure
Aging
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome
Al-Raqad Syndrome
Alzheimer Disease Mitochondrial
Aniridia 1
Anorexia Nervosa 1
Ataxia and Polyneuropathy, Adult-Onset
Autism
Autism Spectrum Disorder
Autonomic Dysfunction
Autosomal Dominant Progressive External Ophthalmoplegia
Axonal Neuropathy
Behr Syndrome
Blood Group--Ahonen
Cardioencephalomyopathy
Carpal Tunnel Syndrome
Cerebral Folate Deficiency
Cerebritis
Cerebrotendinous Xanthomatosis
Charcot-Marie-Tooth Disease
Chronic Progressive External Ophthalmoplegia
Coenzyme Q10 Deficiency Disease
Combined Oxidative Phosphorylation Deficiency
Complex Regional Pain Syndrome
Congenital Cataract-Hypertrophic Cardiomyopathy-Mitochondrial Myopathy Syndrome
Cortical Blindness
Cranial Nerve Disease
Cyclic Vomiting Syndrome
Cystinuria
Diabetes and Deafness, Maternally Inherited
Diphyllobothriasis
Dysphagia
Dystonia
Dystrophinopathies
Encephalomyopathy
End Stage Renal Failure
Epilepsy
Fatal Infantile Cytochrome C Oxidase Deficiency
Fatal Infantile Encephalocardiomyopathy
Focal Segmental Glomerulosclerosis
Growth Hormone Deficiency
Hydrops, Lactic Acidosis, and Sideroblastic Anemia
Hyperphenylalaninemia
Hypertrichosis
Hypertrophic Cardiomyopathy
Hypertrophic Olivary Degeneration
Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1
Inherited Metabolic Disorder
Intestinal Pseudo-Obstruction
Kearns-Sayre Syndrome
Lactic Acidosis
Leber Hereditary Optic Neuropathy
Leber Optic Atrophy
Leber Optic Atrophy and Dystonia
Leigh Syndrome
Leigh Syndrome with Leukodystrophy
Malignant Hyperthermia
Malignant Hyperthermia Susceptibility
Maternally-Inherited Progressive External Ophthalmoplegia
Microphthalmia
Mitochondrial Complex I Deficiency
Mitochondrial Complex Iv Deficiency
Mitochondrial Disorders
Mitochondrial Dna-Associated Leigh Syndrome and Narp
Mitochondrial Dna Depletion Syndrome 1
Mitochondrial Dna Depletion Syndrome 4a
Mitochondrial Dna Depletion Syndrome 7
Mitochondrial Encephalomyopathy
Mitochondrial Myopathy
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes
Mitochondrial Neurogastrointestinal Encephalomyopathy
Mononeuropathy of the Median Nerve, Mild
Myoclonic Epilepsy Associated with Ragged-Red Fibers
Myopathy
Myopathy, Lactic Acidosis, and Sideroblastic Anemia
Myotonic Dystrophy
Neuropathy
Ocular Motility Disease
Optic Nerve Disease
Paine Syndrome
Parkinson Disease 6, Autosomal Recessive Early-Onset
Pearson Marrow-Pancreas Syndrome
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4
Ptosis
Pulmonary Edema
Pyruvate Dehydrogenase E1-Alpha Deficiency
Reflex Sympathetic Dystrophy
Rrm2b-Related Mitochondrial Disease
Sengers Syndrome
Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis
Sparganosis
Spastic Paraplegia 7, Autosomal Recessive
Spinocerebellar Atrophy
Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related
Succinate-Coa Ligase Deficiency
Tooth Disease
Wolfram Syndrome
Xanthomatosis
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