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Mitochondrial Encephalomyopathy
Informaţii despre
Nume
Mitochondrial Encephalomyopathy
Pagina Web
www.malacards.org
Clasificare anatomică Malacards
Boli musculare
Vezi şi
Boli A-Z
Acquired Idiopathic Sideroblastic Anemia
Aging
Amelogenesis Imperfecta, Type Iv
Amenorrhea
Aminoacidopathies
Aniridia 1
Anorexia Nervosa 1
Arthrochalasia Ehlers-Danlos Syndrome
Ataxia and Polyneuropathy, Adult-Onset
Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus
Atrioventricular Block
Bleeding Disorder, Platelet-Type, 11
Blood Group--Ahonen
Blood Group, I System
Cataract
Cercarial Dermatitis
Cerebral Hemorrhage
Cerebritis
Choroiditis
Chronic Progressive External Ophthalmoplegia
Coenurosis
Combined Oxidative Phosphorylation Deficiency 6
Cortical Blindness
Cranial Nerve Disease
Deafness, Aminoglycoside-Induced
Deafness, Nonsyndromic Sensorineural, Mitochondrial
Dementia
Diabetes and Deafness, Maternally Inherited
Diabetes Mellitus
Diphyllobothriasis
Early Myoclonic Encephalopathy
Encephalitis
Encephalomyopathy
Endotheliitis
Epilepsy
Familial Colorectal Cancer
Fanconi Syndrome
Fatal Infantile Encephalocardiomyopathy
Focal Segmental Glomerulosclerosis
Fumarase Deficiency
Genetic Recurrent Myoglobinuria
Gonadal Disease
Growth Hormone Deficiency
Herpes Simplex
Herpes Simplex Encephalitis
Hypertrophic Cardiomyopathy
Hypoparathyroidism
Hypopituitarism
Isolated Complex Iii Deficiency
Kearns-Sayre Syndrome
Lactic Acidosis
Leber Hereditary Optic Neuropathy
Leber Optic Atrophy
Leber Optic Atrophy and Dystonia
Leigh Syndrome
Leukodystrophy
Lice Infestation
Lissencephaly 1
Maternally-Inherited Progressive External Ophthalmoplegia
Mitochondrial Complex Iv Deficiency
Mitochondrial Disorders
Mitochondrial Dna-Associated Leigh Syndrome and Narp
Mitochondrial Dna Depletion Syndrome 4a
Mitochondrial Metabolism Disease
Mitochondrial Myopathy
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes
Muscular Dystrophy
Mutism
Myasthenic Syndrome, Congenital, 10
Myiasis
Myoclonic Cerebellar Dyssynergia
Myoclonic Epilepsy Associated with Ragged-Red Fibers
Myoclonus
Myoglobinuria
Myoglobinuria, Recurrent
Myotonic Dystrophy
Open-Angle Glaucoma
Optic Nerve Disease
Pancreatitis
Parkinson Disease 6, Autosomal Recessive Early-Onset
Pearson Marrow-Pancreas Syndrome
Polyhydramnios
Retinal Detachment
Retinitis
Retinoblastoma
Ring Chromosome 18
Sensorineural Hearing Loss
Sleep Apnea
Sparganosis
Superior Mesenteric Artery Syndrome
Taeniasis
Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6
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