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Nume Sensorineural Hearing Loss
Pagina Web www.malacards.org
Clasificari ICD10 Hearing loss, unspecified; Sensorineural hearing loss, bilateral; Sensorineural hearing loss, unilateral with unrestricted hearing on the contralateral side; Sensorineural hearing loss, unspecified
Clasificare anatomică Malacards Boli ale urechii

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Boli A-Z 3-Methylglutaconic Aciduria, Type V Acoustic Neuroma Acute Myocardial Infarction Adenocarcinoma Aging Alcohol Abuse Allan-Herndon-Dudley Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, Autosomal Dominant Alport Syndrome, X-Linked Al-Raqad Syndrome Amelogenesis Imperfecta Amenorrhea Amyloidosis Aneurysm Aniridia 1 Anorexia Nervosa 1 Anosmia Antiphospholipid Syndrome Aortitis Arachnoid Cysts Arachnoiditis Arteries, Anomalies of Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aseptic Meningitis Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Audiogenic Seizures Auditory Neuropathy, Autosomal Dominant, 1 Auditory Neuropathy Spectrum Disorder Auditory System Disease Autism Autoimmune Disease Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna Autosomal Recessive Nonsyndromic Deafness Autosomal Recessive Nonsyndromic Deafness 3 Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb Beckwith-Wiedemann Syndrome Bjornstad Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I 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 Bone Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brachydactyly Brain Injury Brainstem Auditory Evoked Responses Branchiootic Syndrome 1 Brucellosis Cardiospondylocarpofacial Syndrome Cataract Central Nervous System Origin Vertigo Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy, and Sensorineural Hearing Loss Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy and Sensorinural Hearing Loss Cerebellopontine Angle Tumor Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 Cerebritis Cerebrovascular Disease Cervicitis Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease, X-Linked Recessive, 5 Cholesteatoma Chorioamnionitis Choroiditis Chronic Progressive External Ophthalmoplegia Cleft Lip Cleft Lip/palate Cleidocranial Dysplasia Spectrum Disorder Clouston Syndrome Coffin-Lowry Syndrome Collagen Disease Combined Oxidative Phosphorylation Deficiency 9 Combined Pituitary Hormone Deficiency Cone Dystrophy Cone-Rod Dystrophy 2 Congenital Contractures Congenital Cytomegalovirus Congenital Erosive and Vesicular Dermatosis Congenital Syphilis Congenital Toxoplasmosis Connective Tissue Disease Conversion Disorder Corneal Dystrophy Craniosynostosis with Fibular Aplasia Cytomegalovirus Infection Deafness, Autosomal Dominant 11 Deafness, Autosomal Dominant 12 Deafness, Autosomal Dominant 13 Deafness, Autosomal Dominant 17 Deafness, Autosomal Dominant 22 Deafness, Autosomal Dominant 24 Deafness, Autosomal Dominant 2a Deafness, Autosomal Dominant 36 Deafness, Autosomal Dominant 48 Deafness, Autosomal Dominant 5 Deafness, Autosomal Dominant 52 Deafness, Autosomal Dominant 6 Deafness, Autosomal Dominant 69 Deafness, Autosomal Dominant 9 Deafness, Autosomal Recessive 12 Deafness, Autosomal Recessive 16 Deafness, Autosomal Recessive 1a Deafness, Autosomal Recessive 1b Deafness, Autosomal Recessive 2 Deafness, Autosomal Recessive 20 Deafness, Autosomal Recessive 23 Deafness, Autosomal Recessive 26 Deafness, Autosomal Recessive 28 Deafness, Autosomal Recessive 3 Deafness, Autosomal Recessive 30 Deafness, Autosomal Recessive 31 Deafness, Autosomal Recessive 37 Deafness, Autosomal Recessive 40 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct Deafness, Autosomal Recessive 59 Deafness, Autosomal Recessive 6 Deafness, Autosomal Recessive 63 Deafness, Autosomal Recessive 7 Deafness, Autosomal Recessive 83 Deafness, Autosomal Recessive 85 Deafness, Autosomal Recessive 9 Deafness, Autosomal Recessive 93 Deafness, X-Linked 2 Dentin Dysplasia, Type Ii Dermoid Cyst Dfnb1 Diabetes Mellitus Dilated Cardiomyopathy Donnai-Barrow Syndrome Dyslexia Dysostosis Ear Malformation Ehrlichiosis Encephalomyopathy Encephalopathy Endotheliitis Entropion Epstein Syndrome Erythrokeratodermia Variabilis Et Progressiva 1 Exfoliation Syndrome Facial Paralysis Factitious Disorder Familial Adenomatous Polyposis Fanconi Anemia, Complementation Group E Fibromatosis Fibromatosis, Gingival, with Progressive Deafness Focal Segmental Glomerulosclerosis Gastric Cancer Genitopatellar Syndrome Germ Cells Tumors Gingival Fibromatosis Gingivitis Glaucoma-Related Pigment Dispersion Syndrome Glucocorticoid Resistance, Generalized Gonadal Dysgenesis Headache Head Injury Hemangioma Hemifacial Hyperplasia Hemophagocytic Lymphohistiocytosis Hepatitis Hepatitis C Herpes Zoster Hinman Syndrome Histiocytosis Histiocytosis-Lymphadenopathy Plus Syndrome Hodgkin's Lymphoma, Nodular Sclerosis Human Monocytic Ehrlichiosis Hyperacusis Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant Hypercholesterolemia, Autosomal Dominant, 3 Hyperglycemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Retinopathy Hypertrophic Cardiomyopathy Hypocomplementemic Urticarial Vasculitis Hypoglossia-Hypodactylia Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypopituitarism Hypotonia Hypotrichosis-Deafness Syndrome Ichthyosis Inner Ear Disease Interstitial Keratitis Interstitial Nephritis Intracranial Hypotension Iritis Ischemia Juvenile Pilocytic Astrocytoma Kawasaki Disease Kearns-Sayre Syndrome Kid Syndrome Knuckle Pads Knuckle Pads, Leukonychia, and Sensorineural Deafness Labyrinthitis Lactic Acidosis Langerhans Cell Histiocytosis Laryngomalacia Lassa Fever Left Ventricular Noncompaction Linear Iga Disease Lupus Erythematosus Lyme Disease Malignant Hypertension Malignant Spiradenoma Mastoiditis Meckel Syndrome, Type 1 Medulloblastoma Meningitis Meningococcal Meningitis Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, and Keratoderma Mental Retardation, X-Linked, Syndromic, Martin-Probst Type Microcephaly Microcytic Anemia Microscopic Polyangiitis Middle Ear Cholesterol Granuloma Middle Ear Disease Miliary Tuberculosis Mitochondrial Encephalomyopathy Mixed Connective Tissue Disease Mondini Dysplasia Muckle-Wells Syndrome Mucopolysaccharidosis-Plus Syndrome Multiple Sclerosis Mumps Musical Perfect Pitch Myelodysplastic Syndrome Myocardial Infarction Myopathy Myringitis Bullosa Hemorrhagica Nail-Patella Syndrome Nasopharyngeal Carcinoma Nasopharyngitis Neonatal Jaundice Neonatal Respiratory Failure Nephrocalcinosis Nephrotic Syndrome Neuritis Neurofibromatosis, Type Iv, of Riccardi Neuroma Neuronitis Neuropathy Neurosarcoidosis Non-Involuting Congenital Hemangioma Nonsyndromic Deafness Non-Syndromic Genetic Deafness Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Otitis Externa Otitis Media Otosclerosis Paraganglioma Patulous Eustachian Tube Pendred Syndrome Perilymphatic Fistula Periodontitis Perrault Syndrome Phace Syndrome Pili Torti Pilocytic Astrocytoma Pneumococcal Meningitis Polyarteritis Nodosa Polyneuropathy Pontine Hemorrhage Premature Ovarian Failure 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 Dominant 4 Propionic Acidemia Pseudoainhum Pseudohypoparathyroidism Psoriatic Arthritis Ptosis Pulmonary Hypertension Radioulnar Synostosis Relapsing Polychondritis Renal Tubular Acidosis Renal Tubular Acidosis, Distal, Autosomal Recessive Retinitis Retinitis Pigmentosa Rheumatoid Arthritis Saethre-Chotzen Syndrome Scleritis Scrub Typhus Secondary Syphilis Sickle Cell Disease Siderosis Silver-Russell Syndrome Sinusitis Skin Disease Sleep Apnea Spasticity Spastic Paraparesis Split Hand Split Hand-Foot Malformation Spondylitis Spondyloarthropathy 1 Spontaneous Intracranial Hypotension Sudden Sensorineural Hearing Loss Superficial Siderosis Superficial Siderosis of the Central Nervous System Superior Semicircular Canal Dehiscence Suppurative Otitis Media Susac Syndrome Sveinsson Chorioretinal Atrophy Sympathetic Ophthalmia Synostosis Syphilis Systemic Lupus Erythematosus Temporal Arteritis Thyroiditis Tooth Disease Toxoplasmoză Traumatic Brain Injury Tuberculous Meningitis Uremia Usher Syndrome Usher Syndrome Type 2 Usher Syndrome, Type I Usher Syndrome, Type Id Usher Syndrome, Type if Usher Syndrome, Type Ig Usher Syndrome, Type Iic Usher Syndrome, Type Iid Usher Syndrome, Type Iiia Uveal Coloboma-Cleft Lip and Palate-Intellectual Disability Varicose Veins Vasculitis Vertebrobasilar Insufficiency Vestibular Disease Vici Syndrome Viral Labyrinthitis Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Vogt-Koyanagi-Harada Disease Vohwinkel Syndrome Walker-Warburg Syndrome Wells Syndrome Wernicke Encephalopathy West Nile Virus Wolfram Syndrome Wolfram Syndrome 1