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Boli A-Z | | 3-Hydroxyisobutyryl-Coa Hydrolase Deficiency
3-Methylglutaconic Aciduria, Type Iii
3-Methylglutaconic Aciduria, Type V
Aging
Alexander Disease
Al-Raqad Syndrome
Alzheimer Disease Mitochondrial
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
Autism
Autism Spectrum Disorder
Autosomal Dominant Progressive External Ophthalmoplegia
Axonal Neuropathy
Basal Ganglia Calcification
Blood Group--Ahonen
Blood Group, Dombrock System
Body Mass Index Quantitative Trait Locus 10
Body Mass Index Quantitative Trait Locus 11
Body Mass Index Quantitative Trait Locus 12
Body Mass Index Quantitative Trait Locus 14
Body Mass Index Quantitative Trait Locus 18
Body Mass Index Quantitative Trait Locus 4
Body Mass Index Quantitative Trait Locus 7
Body Mass Index Quantitative Trait Locus 8
Body Mass Index Quantitative Trait Locus 9
Burns
Cardioencephalomyopathy
Cardiomyopathy, Infantile Histiocytoid
Carrion's Disease
Cataract
Cercarial Dermatitis
Cerebral Creatine Deficiency Syndrome 1
Cerebritis
Chronic Fatigue Syndrome
Chronic Progressive External Ophthalmoplegia
Coenzyme Q10 Deficiency Disease
Combined Oxidative Phosphorylation Deficiency 19
Cortical Blindness
Cranial Nerve Disease
Crouzon Syndrome
Cyclic Vomiting Syndrome
Deafness, Aminoglycoside-Induced
Deafness, Nonsyndromic Sensorineural, Mitochondrial
Dementia
Diabetes and Deafness, Maternally Inherited
Diabetic Polyneuropathy
Dilated Cardiomyopathy
Diphyllobothriasis
Dystrophinopathies
Early Myoclonic Encephalopathy
Encephalitis
Encephalomyopathy
Encephalopathy
Epilepsy
Fanconi Anemia, Complementation Group E
Fatal Infantile Cytochrome C Oxidase Deficiency
Fatal Infantile Encephalocardiomyopathy
Gastroparesis
Growth Hormone Deficiency
Headache
Hepatitis
Hereditary Ataxia
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy
Hypertrophic Cardiomyopathy
Hypertrophic Olivary Degeneration
Hypogonadism
Isolated Atp Synthase Deficiency
Kearns-Sayre Syndrome
Lactic Acidosis
Lateral Sclerosis
Leber Hereditary Optic Neuropathy
Leber Optic Atrophy
Leber Optic Atrophy and Dystonia
Leigh Syndrome
Lipomatosis
Liver Disease
Malignant Hyperthermia
Malignant Hyperthermia Susceptibility
Maternally-Inherited Progressive External Ophthalmoplegia
Microcephaly
Mitochondrial Complex I Deficiency
Mitochondrial Complex Iv Deficiency
Mitochondrial Complex V Deficiency
Mitochondrial Dna-Associated Leigh Syndrome and Narp
Mitochondrial Dna Depletion Syndrome 1
Mitochondrial Dna Depletion Syndrome 3
Mitochondrial Dna Depletion Syndrome 4a
Mitochondrial Dna Depletion Syndrome 7
Mitochondrial Encephalomyopathy
Mitochondrial Metabolism Disease
Mitochondrial Myopathy
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes
Mitochondrial Neurogastrointestinal Encephalomyopathy
Mitochondrial Neurogastrointestinal Encephalopathy Disease
Mitochondrial Non-Syndromic Sensorineural Deafness
Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly
Multiple Sclerosis
Multiple Symmetrical Lipomatosis
Muscular Dystrophy
Myasthenic Syndrome, Congenital, 10
Myoclonic Epilepsy Associated with Ragged-Red Fibers
Myoclonus
Myoclonus Epilepsy
Myopathy
Myopathy, Lactic Acidosis, and Sideroblastic Anemia
Myotonia
Neuronitis
Neuropathy
Neutropenia
Ocular Motility Disease
Optic Nerve Disease
Parkinson Disease 6, Autosomal Recessive Early-Onset
Parkinson Disease, Mitochondrial
Pearson Marrow-Pancreas Syndrome
Polycystic Ovary Syndrome
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 1
Pulmonary Hypertension
Renal Tubular Acidosis
Retinitis
Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis
Sideroblastic Anemia
Sparganosis
Spasticity
Spastic Paraparesis
Spastic Paraplegia 7, Autosomal Recessive
Spondyloocular Syndrome
Stereotypic Movement Disorder
Undifferentiated Pleomorphic Sarcoma
Vici Syndrome
Wolfram Syndrome |
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