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Nume Branchiootic Syndrome 1
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Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificare anatomică Malacards Boli ale urechii
Boli din aceeaşi familie Branchiootic Syndrome 2; Branchiootic Syndrome 3

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Boli A-Z 3-Methylglutaconic Aciduria 3-Methylglutaconic Aciduria, Type Iv 3-Methylglutaconic Aciduria with Deafness, Encephalopathy, and Leigh-Like Syndrome 46,xx Sex Reversal 1 46,xy Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy Abcd Syndrome Acanthosis Nigricans Aceruloplasminemia Achalasia Acoustic Neuroma Acroosteolysis Adenosine Deaminase Deficiency Agammaglobulinemia Aging Agnosia Albinism Albinism-Deafness Syndrome Albinism, Ocular, Type I Albinism, Ocular, with Late-Onset Sensorineural Deafness Albinism, Ocular, with Sensorineural Deafness Alexia Alopecia Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amusia Amyloidosis Aneurysm Anhidrosis Aniridia 1 Ankylosis Anorexia Nervosa 1 Antenatal Bartter Syndrome Antiphospholipid Syndrome Aphasia Arachnoid Cysts Arachnoiditis Argininosuccinic Aciduria Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Arts Syndrome Asperger Syndrome Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Deafness-Retardation Syndrome Ataxia-Oculomotor Apraxia 3 Ataxia with Vitamin E Deficiency Athetosis Audiogenic Seizures Auditory Agnosia Aural Atresia, Congenital Autism Autism Spectrum Disorder Autosomal Dominant Cerebellar Ataxia Autosomal Dominant Nonsyndromic Deafness Autosomal Dominant Optic Atrophy Plus Syndrome Autosomal Recessive Nonsyndromic Deafness Autosomal Recessive Nonsyndromic Deafness 3 Autosomal Recessive Nonsyndromic Deafness 86 Autosomal Recessive Non-Syndromic Intellectual Disability Ayazi Syndrome Ayme-Gripp Syndrome Bacterial Meningitis Baraitser-Winter Syndrome 1 Bardet-Biedl Syndrome Barth Syndrome Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness Bartter Syndrome, Type 4b, Neonatal, with Sensorineural Deafness Basal Ganglia Calcification Basilar Artery Occlusion Biotinidase Deficiency Bjornstad Syndrome Bleeding Disorder, Platelet-Type, 11 Blepharophimosis Blepharospasm 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 Bohring-Opitz Syndrome Bone Fracture Brachycephaly, Deafness, Cataract, Microstomia, and Mental Retardation Brachydactyly Brainstem Auditory Evoked Responses Branchial Arch Defects Branchial Cleft Anomalies Branchiogenic-Deafness Syndrome Branchiooculofacial Syndrome Branchiootic Syndrome Branchiootic Syndrome 2 Branchiootic Syndrome 3 Branchiootorenal/branchiootic Syndrome Branchiootorenal Syndrome Branchiootorenal Syndrome 1 Brown-Vialetto-Van Laere Syndrome Brugada Syndrome Buschke-Ollendorff Syndrome Calcinosis Candidiasis Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism Cataract Cellulitis Central Nervous System Origin Vertigo Central Retinal Vein Occlusion Central Sleep Apnea Cerebellar Astrocytoma Cerebellar Ataxia and Neurosensory Deafness Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant Cerebellar Degeneration Cerebellar Hypoplasia Cerebellofaciodental Syndrome Cerebellopontine Angle Meningioma Cerebellopontine Angle Tumor Cerebral Folate Deficiency Cerebral Palsy Cerebritis Cervical Rib Cervicitis Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease and Deafness Charge Syndrome Choanal Atresia, Posterior Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction Choroideremia Choroideremia, Deafness, and Mental Retardation Chromosome 8p23.1 Deletion Chronic Inflammatory Demyelinating Polyradiculoneuropathy Chronic Mucocutaneous Candidiasis Chudley-Mccullough Syndrome Churg-Strauss Syndrome Cleft Lip Cleft Lip/palate Cleft Soft Palate Cleft Tongue Cloacal Exstrophy Clouston Syndrome Coffin-Lowry Syndrome Cohen Syndrome Colchicine Resistance Collagen Disease Coloboma, Ocular, Autosomal Dominant Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, and Deafness Color Blindness Commissural Lip Pits Communicating Hydrocephalus Complex Regional Pain Syndrome Cone Dystrophy Congenital Cytomegalovirus Congenital Disorder of Glycosylation, Type Iic Congenital Disorder of Glycosylation, Type in Congenital Generalized Lipodystrophy Congenital Ichthyosiform Erythroderma Congenital Rubella Corneal Disease Corneal Dystrophy Corneal Dystrophy and Perceptive Deafness Corneal Dystrophy, Band-Shaped Corneal Dystrophy, Fleck Corneal Endothelial Dystrophy Corneal Neovascularization Cortical Deafness Craniofacial-Deafness-Hand Syndrome Craniofrontonasal Syndrome Craniosynostosis Craniosynostosis with Fibular Aplasia Crest Syndrome Creutzfeldt-Jakob Disease Cryptococcal Meningitis Cumulative Trauma Disorders Cutaneous Candidiasis Cutis Laxa, Autosomal Recessive, Type Iiia Cutis Verticis Gyrata Cystathioninuria Cytomegalovirus Infection Dacryocystitis Dandy-Walker Syndrome Deafness, Aminoglycoside-Induced Deafness and Myopia Deafness, Autosomal Dominant 1 Deafness, Autosomal Dominant 10 Deafness, Autosomal Dominant 11 Deafness, Autosomal Dominant 15 Deafness, Autosomal Dominant 16 Deafness, Autosomal Dominant 25 Deafness, Autosomal Dominant 36 Deafness, Autosomal Dominant 41 Deafness, Autosomal Dominant 48 Deafness, Autosomal Dominant 4a Deafness, Autosomal Dominant 5 Deafness, Autosomal Dominant 50 Deafness, Autosomal Dominant 58 Deafness, Autosomal Dominant 9 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 3 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 53 Deafness, Autosomal Recessive Deafness, Autosomal Recessive 12 Deafness, Autosomal Recessive 13 Deafness, Autosomal Recessive 14 Deafness, Autosomal Recessive 15 Deafness, Autosomal Recessive 16 Deafness, Autosomal Recessive 17 Deafness, Autosomal Recessive 18a Deafness, Autosomal Recessive 1a Deafness, Autosomal Recessive 1b Deafness, Autosomal Recessive 2 Deafness, Autosomal Recessive 21 Deafness, Autosomal Recessive 22 Deafness, Autosomal Recessive 23 Deafness, Autosomal Recessive 26 Deafness, Autosomal Recessive 29 Deafness, Autosomal Recessive 31 Deafness, Autosomal Recessive 35 Deafness, Autosomal Recessive 37 Deafness, Autosomal Recessive 46 Deafness, Autosomal Recessive 48 Deafness, Autosomal Recessive 49 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct Deafness, Autosomal Recessive 51 Deafness, Autosomal Recessive 63 Deafness, Autosomal Recessive 66 Deafness, Autosomal Recessive 74 Deafness, Autosomal Recessive 79 Deafness, Autosomal Recessive 8 Deafness, Autosomal Recessive 98 Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Deafness, Congenital, with Onychodystrophy, Autosomal Dominant Deafness-Infertility Syndrome Deafness, Nonsyndromic, Modifier 1 Deafness-Oligodontia Syndrome Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Deafness, Unilateral Deafness with Labyrinthine Aplasia Microtia and Microdontia Deafness, X-Linked 1 Deafness, X-Linked 2 Deafness, X-Linked 4 Dedifferentiated Liposarcoma Dementia Dental Caries Dermatophytosis Dfnb1 Dfnx1 Nonsyndromic Hearing Loss and Deafness Diabetes and Deafness, Maternally Inherited Diabetes Insipidus Diabetes Mellitus Diarrhea Digeorge Syndrome Discoid Lupus Erythematosus Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation Dnmt1-Related Dementia, Deafness, and Sensory Neuropathy Down Syndrome Dyslexia Dysostosis Dysphasia, Familial Developmental Dystonia Ear Malformation Echolalia Ectodermal Dysplasia Elective Mutism Ellis-Van Creveld Syndrome Encephalitis Encephalomyopathy Encephalopathy Endemic Goiter Endocarditis Endolymphatic Sac Tumor Endotheliitis Epidermoid Cysts Epidermolysis Bullosa Epilepsy Epithelial Recurrent Erosion Dystrophy Epstein Syndrome Exfoliation Syndrome Facial Paralysis Fainting Familial Deafness Familial Hemiplegic Migraine Familial Thyroid Dyshormonogenesis Fanconi Anemia, Complementation Group E Fazio-Londe Disease Fissured Tongue Focal Epilepsy Focal Segmental Glomerulosclerosis Fountain Syndrome Fraser Syndrome 1 Frontotemporal Dementia Gapo Syndrome Gaucher Disease, Type I Gestational Diabetes Gilles De La Tourette Syndrome Glaucoma-Related Pigment Dispersion Syndrome Glomerulonephritis Glucose Intolerance Glucose Transporter Type 1 Deficiency Syndrome Goiter Gonadal Dysgenesis Growth Hormone Deficiency Gupta Patton Syndrome Head Injury Helix Syndrome Hemiplegic Migraine Hemosiderosis Hepatic Adenomas, Familial Hepatitis Hepatoblastoma Hereditary Hearing Loss and Deafness Hereditary Sensory Neuropathy Herpes Simplex Herpes Simplex Encephalitis Herpes Zoster Herpes Zoster Ophthalmicus Histiocytosis Holoprosencephaly Hydrocephalus Hydronephrosis Hyperacusis Hyperglycemia Hyperinsulinism Hyperparathyroidism Hyperprolinemia Hypertelorism Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrichosis Hypertrophic Cardiomyopathy Hypervitaminosis D Hypoaldosteronism Hypogonadism Hypohidrosis Hypomelanotic Disorder Hypoparathyroidism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatemia Hyporeninemic Hypoaldosteronism Hypospadias Hypotonia Hypotrichosis Hypotrichosis-Deafness Syndrome Hypoxia Ichthyosis Ichthyosis, Congenital, Autosomal Recessive 1 Ichthyosis Prematurity Syndrome Immune Suppression Infertility Interstitial Keratitis Interstitial Nephritis Intestinal Pseudo-Obstruction Intracranial Hypertension Iridocorneal Endothelial Syndrome Iridocyclitis Iritis Kallmann Syndrome Kearns-Sayre Syndrome Keratitis, Hereditary Keratoderma, Palmoplantar, with Deafness Keratopathy Keratosis Keratosis Follicularis Spinulosa Decalvans Kernicterus Kid Syndrome Klippel-Feil Syndrome Labyrinthitis Lactic Acidosis Landau-Kleffner Syndrome Lassa Fever Leigh Syndrome Lens Disease Leukemia Leukodystrophy Lichen Planus Lichtenstein-Knorr Syndrome Limb-Girdle Muscular Dystrophy Lipodystrophy Lipodystrophy, Partial, Acquired Locked-in Syndrome Long Qt Syndrome Lubinsky Syndrome Lupus Erythematosus Lymphoma Male Infertility Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome Marshall Syndrome Mast Cell Activation Syndrome Mastoiditis Medulloblastoma Meester-Loeys Syndrome Megaloblastic Anemia Melanoma, Cutaneous Malignant 1 Meningitis Meningococcal Infection Meningococcal Meningitis Mental Retardation, X-Linked, Syndromic, Martin-Probst Type Mesomelia Metabolic Acidosis Microcephaly Microcytic Anemia Microphthalmia Microtia Microtia with Meatal Atresia and Conductive Deafness Middle Ear Disease Miliary Tuberculosis Mitochondrial Encephalomyopathy Mitochondrial Myopathy Mohr-Tranebjaerg Syndrome Mondini Dysplasia Mowat-Wilson Syndrome Muckle-Wells Syndrome Muir-Torre Syndrome Multiple Epiphyseal Dysplasia Multiple Personality Disorder Multiple Sclerosis Mumps Muscular Dystrophy Muscular Dystrophy, Limb-Girdle, Type 2c Mutism Myelocystocele Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders Myoclonus Myoclonus Epilepsy Myopathy Myopia Myositis Myositis Ossificans Myotonia Myxedema Nail Disorder, Nonsyndromic Congenital, 9 Narcolepsy Nephrocalcinosis Nephrotic Syndrome Neuroma Neuronitis Neuropathy Neuropathy, Hereditary Motor and Sensory, with Deafness, Mental Retardation, and Absent Sensory Large Myelinated Fibers Neurosyphilis Nevus of Ota Nodular Goiter Nonsyndromic Deafness Nonsyndromic Hearing Loss and Deafness, Dfna3 Nonsyndromic Hearing Loss and Deafness, Dfnb1 Nonsyndromic Hearing Loss and Deafness, Mitochondrial Norrie Disease Ocular Albinism Oculocutaneous Albinism Olivopontocerebellar Atrophy Omphalocele, Exstrophy of the Cloaca, Imperforate Anus, and Spinal Defects Complex Oral Squamous Cell Carcinoma Osteitis Fibrosa Osteopetrosis Otitis Media Otof-Related Deafness Otosclerosis Pachygyria Paine Syndrome Palatopharyngeal Incompetence Parotitis Pedophilia Pellagra Pemphigus Pemphigus Vegetans Pendred Syndrome Perifolliculitis Capitis Abscedens Et Suffodiens, Familial Perilymphatic Fistula Periodic Fever, Aphthous Stomatitis, Pharyngitis and Adenitis Peripheral T-Cell Lymphoma Perrault Syndrome Personality Disorder Pervasive Developmental Disorder Peters-Plus Syndrome Phelan-Mcdermid Syndrome Pili Torti Pituitary Hormone Deficiency, Combined, 2 Pityriasis Lichenoides Pityriasis Lichenoides Chronica Placenta Accreta Pneumococcal Meningitis Pneumonia Polydactyly Polyhydramnios Polyneuropathy Polyradiculoneuropathy Porokeratotic Eccrine Ostial and Dermal Duct Nevus Postural Hypotension Preauricular Sinus Premature Ovarian Failure 1 Primary Optic Atrophy Progressive Bulbar Palsy Prolidase Deficiency Proliferative Glomerulonephritis Propionic Acidemia Prune Belly Syndrome Pseudohermaphroditism Pseudoxanthoma Elasticum Psoriasis Psoriasis 13 Ptosis Pulmonic Stenosis Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency Rapp-Hodgkin Syndrome Renal Dysplasia Renal Tubular Acidosis Reticular Dysgenesis Retinal Degeneration Retinal Vascular Disease Retinal Vein Occlusion Retinitis Retinitis Pigmentosa Riboflavin Transporter Deficiency Riboflavin Transporter Deficiency Neuronopathy Ring Chromosome 4 Rocky Mountain Spotted Fever Rosai-Dorfman Disease Rubella Santos Mateus Leal Syndrome Sapho Syndrome Sarcoidosis 2 Schaap Taylor Baraitser Syndrome Schinzel Giedion Syndrome Schizophrenia Schlegelberger Grote Syndrome Scoliosis Secondary Syphilis Secretory Diarrhea Seizure Disorder Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance Semilobar Holoprosencephaly Senior-Løken Syndrome Sensorineural Hearing Loss Sensory Neuropathy Type 1 Severe Combined Immunodeficiency Shigellosis Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Siderosis Skeletal Dysplasias Skin Disease Sleep Apnea Smith-Magenis Syndrome Sparganosis Spastic Ataxia, Charlevoix-Saguenay Type Spasticity Spastic Paraparesis Spastic Paraparesis and Deafness Specific Language Impairment Spinocerebellar Ataxia, Autosomal Recessive 3 Splenomegaly Split Foot Split Hand Split Hand-Split Foot Malformation Spondylarthropathy Spondyloocular Syndrome Spotted Fever Squamous Cell Carcinoma Status Epilepticus Strabismus Streptococcal Meningitis Striatal Degeneration, Autosomal Dominant 2 Subacute Bacterial Endocarditis Subdural Empyema Sudden Sensorineural Hearing Loss Superficial Siderosis Superficial Siderosis of the Central Nervous System Suppurative Otitis Media Susac Syndrome Sympathetic Ophthalmia Synostosis Syphilis Systemic Lupus Erythematosus Teeth Present at Birth Telangiectasis Telecanthus Temporal Arteritis Tertiary Syphilis Testicular Cancer Thrombasthenia Thrombocytopenia Thyroiditis Thyrotoxic Periodic Paralysis 2 Tietz Albinism-Deafness Syndrome Tooth Disease Trichostasis Spinulosa Tune Deafness Usher Syndrome Usher Syndrome, Type I Usher Syndrome, Type Ic Usher Syndrome, Type if Usher Syndrome, Type Iic Usher Syndrome, Type Ij Uveitis Van Der Woude Syndrome 1 Vascular Disease Vasculitis Vein of Galen Aneurysm Ventricular Septal Defect Verbal Auditory Agnosia Vertebrobasilar Insufficiency Vertical Talus, Congenital Vestibular Disease Vestibular Neuronitis Vitreoretinal Degeneration Vohwinkel Syndrome Waardenburg's Syndrome Waardenburg Syndrome, Type 2e Waardenburg Syndrome, Type 4c Wells-Jankovic Syndrome Wells Syndrome Wernicke Encephalopathy Wilms Tumor 6 Wolff-Parkinson-White Syndrome Wolf-Hirschhorn Syndrome Wolfram Syndrome Xanthoma Disseminatum X-Linked Charcot-Marie-Tooth Disease X-Linked Disease X-Linked Nonsyndromic Deafness Yemenite Deaf-Blind Hypopigmentation Syndrome