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Nume Encephalomyopathy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Boli din aceeaşi familie Fatal Infantile Encephalomyopathy

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Boli A-Z 3-Methylglutaconic Aciduria, Type V Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Amenorrhea Aminoacidopathies Aneurysm 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 Ataxia-Oculomotor Apraxia 3 Atrioventricular Block Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I System Brainstem Auditory Evoked Responses Branchiootic Syndrome 1 Cataract Cerebral Creatine Deficiency Syndrome 3 Cerebral Hemorrhage Cerebritis Chorioretinitis Choroiditis Chronic Inflammatory Demyelinating Polyradiculoneuropathy Combined Oxidative Phosphorylation Deficiency 6 Cortical Blindness Cranial Nerve Disease Cystic Fibrosis Dementia Diabetes Mellitus Diverticulitis Dystonia Eating Disorder Encephalitis Encephalopathy Endocarditis Endotheliitis Epilepsy Fanconi Syndrome Focal Segmental Glomerulosclerosis Fumarase Deficiency Gonadal Disease Growth Hormone Deficiency Hepatic Adenomas, Familial Herpes Simplex Herpes Simplex Encephalitis Hydrocephalus Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypogonadism Hypoparathyroidism Hypopituitarism Intestinal Pseudo-Obstruction Isolated Complex Iii Deficiency Kearns-Sayre Syndrome Lactic Acidosis Leber Hereditary Optic Neuropathy Leber Optic Atrophy Leber Optic Atrophy and Dystonia Leigh Syndrome Leukodystrophy Lipomatosis Lissencephaly 1 Mitochondrial Complex I Deficiency Mitochondrial Complex Ii 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 5 Mitochondrial Encephalomyopathy Mitochondrial Myopathy Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Mitochondrial Myopathy with Diabetes Mitochondrial Neurogastrointestinal Encephalomyopathy Mitochondrial Neurogastrointestinal Encephalopathy Disease Multiple Symmetrical Lipomatosis Muscular Dystrophy Mutism Myoclonic Cerebellar Dyssynergia Myoclonic Epilepsy Associated with Ragged-Red Fibers Myoclonus Myopathy Myotonic Dystrophy Neuropathy Open-Angle Glaucoma Optic Nerve Disease Pancreatitis Parkinson Disease 6, Autosomal Recessive Early-Onset Peritonitis Polyhydramnios Polyradiculoneuropathy Premature Ovarian Failure 1 Refractory Celiac Disease Retinal Detachment Retinitis Retinoblastoma Ring Chromosome 18 Sensorineural Hearing Loss Sleep Apnea Spondylocarpotarsal Synostosis Syndrome Superior Mesenteric Artery Syndrome Syncope Tetraamelia Syndrome, Autosomal Recessive Trigeminal Neuralgia Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6