Informaţii despre

Nume Tooth Disease
Pagina Web www.malacards.org
Clasificari ICD10 Dental caries, unspecified
Clasificare anatomică Malacards Boli bucale; Boli gastrointestinale

Vezi şi

Boli A-Z Acute Disseminated Encephalomyelitis Aging Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Amyotrophic Neuralgia Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Arts Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autonomic Dysfunction Autonomic Neuropathy Autosomal Dominant Charcot-Marie-Tooth Disease Type 2g Autosomal Dominant Intermediate Charcot-Marie-Tooth Autosomal Recessive Intermediate Charcot-Marie-Tooth Disease Axonal Neuropathy Baraitser-Winter Syndrome 1 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brachial Plexus Neuropathy Cataract Cauda Equina Syndrome Centronuclear Myopathy Cerebritis Cervicitis Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease and Deafness Charcot-Marie-Tooth Disease, Axonal, Type 2a1 Charcot-Marie-Tooth Disease, Axonal, Type 2b Charcot-Marie-Tooth Disease, Axonal, Type 2b2 Charcot-Marie-Tooth Disease, Axonal, Type 2d Charcot-Marie-Tooth Disease, Axonal, Type 2e Charcot-Marie-Tooth Disease, Axonal, Type 2f Charcot-Marie-Tooth Disease, Axonal, Type 2i Charcot-Marie-Tooth Disease, Axonal, Type 2j Charcot-Marie-Tooth Disease, Axonal, Type 2k Charcot-Marie-Tooth Disease, Axonal, Type 2l Charcot-Marie-Tooth Disease, Axonal, Type 2n Charcot-Marie-Tooth Disease, Axonal, Type 2p Charcot-Marie-Tooth Disease, Axonal, Type 2t Charcot-Marie-Tooth Disease, Demyelinating, Type 1a Charcot-Marie-Tooth Disease, Demyelinating, Type 1b Charcot-Marie-Tooth Disease, Demyelinating, Type 1c Charcot-Marie-Tooth Disease, Demyelinating, Type 1d Charcot-Marie-Tooth Disease, Demyelinating, Type 1f Charcot-Marie-Tooth Disease, Demyelinating, Type 4f Charcot-Marie-Tooth Disease, Dominant Intermediate a Charcot-Marie-Tooth Disease Type 2a Charcot-Marie-Tooth Disease Type 2a2 Charcot-Marie-Tooth Disease Type 2c Charcot-Marie-Tooth Disease Type 2g Charcot-Marie-Tooth Disease Type 2k Charcot-Marie-Tooth Disease Type 2l Charcot-Marie-Tooth Disease Type 2n Charcot-Marie-Tooth Disease, Type 4a Charcot-Marie-Tooth Disease, Type 4b1 Charcot-Marie-Tooth Disease, Type 4b2 Charcot-Marie-Tooth Disease, Type 4b3 Charcot-Marie-Tooth Disease, Type 4c Charcot-Marie-Tooth Disease, Type 4d Charcot-Marie-Tooth Disease, Type 4h Charcot-Marie-Tooth Disease, Type 4j Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 Charcot-Marie-Tooth Disease, X-Linked Dominant, 6 Charcot-Marie-Tooth Disease, X-Linked Recessive, 5 Charcot-Marie-Tooth Neuropathy Type 1 Charcot-Marie-Tooth Neuropathy Type 2a Chromosomal Triplication Chromosome 17p Duplication Chronic Inflammatory Demyelinating Polyneuropathy Congenital Hypomyelination Neuropathy Cowchock Syndrome Cutis Verticis Gyrata Delusional Disorder Demyelinating Disease Demyelinating Polyneuropathy Dental Caries Distal Hereditary Motor Neuropathies Distal Hereditary Motor Neuropathy, Type V Early-Onset Glaucoma Ehlers-Danlos Syndrome Epilepsy Epithelial Recurrent Erosion Dystrophy Ewing Sarcoma Familial Periodic Paralysis Fanconi Anemia, Complementation Group E Floating-Harbor Syndrome Focal Segmental Glomerulosclerosis Foot Drop Glioma Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency Hantavirus Pulmonary Syndrome Hellp Syndrome Hemophilia Hemophilia a Hereditary Motor and Sensory Neuropathy, Type Iic Hereditary Neuropathies Hereditary Neuropathy with Liability to Pressure Palsy Hereditary Sensory Neuropathy Hereditary Spastic Paraplegia Hypertelorism Hypertrophic Neuropathy of Dejerine-Sottas Hypokalemic Periodic Paralysis, Type 1 Hypomelanotic Disorder Laryngeal Cleft Laryngitis Lateral Sclerosis Leber Optic Atrophy Legius Syndrome Leiomyomatosis Leukemia Lymphoblastic Leukemia Medulloblastoma Melanoma Mitochondrial Complex I Deficiency Mitochondrial Trifunctional Protein Deficiency Mixed Glioma Motor Neuron Disease Motor Peripheral Neuropathy Multiple Sclerosis Muscular Atrophy Muscular Dystrophy Myasthenia Gravis Myopathy Myotonia Myotonia Congenita Narcolepsy Neuritis Neurofibroma Neurofibromatosis, Type Iv, of Riccardi Neuromuscular Disease Neuronitis Neuronopathy, Distal Hereditary Motor, Type Va Neuropathy Neuropathy, Congenital Hypomyelinating or Amyelinating, Autosomal Recessive Neuropathy, Hereditary Motor and Sensory, Russe Type Neuropathy, Hereditary Motor and Sensory, Type Via Neuropathy, Hereditary Motor and Sensory, with Deafness, Mental Retardation, and Absent Sensory Large Myelinated Fibers Neuropathy, Hereditary, with Liability to Pressure Palsies Optic Neuritis Papular Elastorrhexis Paraplegia Pelizaeus-Merzbacher Disease Peripheral Nervous System Disease Pitt-Hopkins Syndrome Polyneuropathy Polyneuropathy Associated with Igm Monoclonal Gammapathy with Anti-Mag Primary Cerebellar Degeneration Primary Optic Atrophy Progressive Muscular Atrophy Pseudomyotonia Purpura Relapsing-Remitting Multiple Sclerosis Restless Legs Syndrome Riboflavin Transporter Deficiency Roussy-Levy Hereditary Areflexic Dystasia Sarcoma Scoliosis Seizures, Benign Familial Neonatal, 1 Sensorineural Hearing Loss Sensory Peripheral Neuropathy Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sleep Apnea Sleep Disorder Spastic Ataxia, Charlevoix-Saguenay Type Spasticity Spinal Muscular Atrophy Spinocerebellar Degeneration Superior Mesenteric Artery Syndrome Thrombotic Thrombocytopenic Purpura Tremor Trigeminal Neuralgia Vertical Talus, Congenital Wallerian Degeneration X-Linked Charcot-Marie-Tooth Disease