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Boli A-Z | | Aging
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome
Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity
Al-Raqad Syndrome
Aminoaciduria
Androgen Insensitivity Syndrome, Mild
Angina Pectoris
Aniridia 1
Anorexia Nervosa 1
Apraxia
Apraxia of Eyelid Opening
Arthrochalasia Ehlers-Danlos Syndrome
Aspiration Pneumonia
Benign Familial Infantile Epilepsy
Blepharophimosis
Blepharospasm
Blood Group--Ahonen
Blood Group, I System
Blood Group, Vel System
Cataract
Cenani-Lenz Syndactyly Syndrome
Centronuclear Myopathy
Charcot-Marie-Tooth Disease
Conn's Syndrome
Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis
Creatine Phosphokinase, Elevated Serum
Cyanosis, Transient Neonatal
Dilated Cardiomyopathy
Dysphagia
Dystonia
Encephalitis
Epilepsy
Familial Periodic Paralyses
Familial Periodic Paralysis
Gas Gangrene
Glycogen Storage Disease Ii
Head Injury
Helix Syndrome
Hepatic Adenomas, Familial
Hyperkalemic Periodic Paralysis
Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1
Hypertrophic Pyloric Stenosis
Hypokalemic Periodic Paralysis, Type 2
Hypoparathyroidism
Infertility
Limbic Encephalitis
Major Affective Disorder 2
Malignant Hyperthermia
Mitochondrial Disorders
Multicentric Reticulohistiocytosis
Multiple Mitochondrial Dysfunctions Syndrome 5
Multiple Sclerosis
Muscle Hypertrophy
Muscle Tissue Disease
Muscular Atrophy
Muscular Dystrophy
Muscular Dystrophy, Duchenne Type
Myasthenia Gravis
Myoclonus
Myoglobinuria
Myoglobinuria, Acute Recurrent, Autosomal Recessive
Myopathy
Myositis
Myotonia Atrophica
Myotonia Congenita
Myotonia Congenita, Autosomal Dominant
Myotonia Congenita, Autosomal Recessive
Myotonia, Potassium-Aggravated
Myotonic Disease
Myotonic Dystrophy
Myotonic Dystrophy 1
Myotonic Dystrophy 2
Myxedema
Nephrolithiasis
Nephrolithiasis, X-Linked Recessive, with Renal Failure
Neuromuscular Disease
Neuronitis
Neuropathy, Hereditary Sensory and Autonomic, Type Iii
Nondystrophic Myotonia
Normokalemic Periodic Paralysis
Paramyotonia Congenita of Von Eulenburg
Periodic Paralyses
Pilomatrixoma
Pneumonia
Polymyositis
Prinzmetal's Variant Angina
Pseudomyotonia
Ptosis
Pyle Disease
Retinitis
Retinitis Pigmentosa
Sarcoidosis 2
Schwartz-Jampel Syndrome, Type 1
Scoliosis
Seizures, Benign Familial Neonatal, 1
Spinal Muscular Atrophy
Strabismus
Syncope
Thyroiditis
Tooth Disease
Undifferentiated Pleomorphic Sarcoma
Wolff-Parkinson-White Syndrome |
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