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Nume Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4
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Boli A-Z Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrioventricular Block Autosomal Dominant Progressive External Ophthalmoplegia Axonal Neuropathy Blood Group--Ahonen Blood Group, I System Cataract Chronic Progressive External Ophthalmoplegia Constipation Encephalopathy Exophthalmos Focal Segmental Glomerulosclerosis Huntington Disease Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hypogonadism Intracranial Hypotension Kearns-Sayre Syndrome Keratopathy Lactic Acidosis Lissencephaly 1 Maternally-Inherited Progressive External Ophthalmoplegia Mitochondrial Metabolism Disease Mitochondrial Myopathy Motor Neuron Disease Multiple Sclerosis Myopathy Neuronitis Neuropathy Pharyngitis Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 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 Recessive 1 Ptosis Retinitis Sensorineural Hearing Loss Spastic Paraplegia 7, Autosomal Recessive Strabismus Third-Degree Atrioventricular Block Woodhouse-Sakati Syndrome