Disease Browser
|
Parent Node: Hearing Loss, Sensorineural (D006319) |
..Starting node ..Deafness, Autosomal Recessive 49 (C565717)
|
Child Nodes:
|
Sister Nodes: |
..Acrootoocular Syndrome (C564866)
|
..Albinism ocular late onset sensorineural deafness (C537043)
|
..Arthrogryposis-like hand anomaly and sensorineural deafness (C535386)
|
..Ataxia, Deafness, and Cardiomyopathy (C565932)
|
..Athabaskan brainstem dysgenesis (C535397)
|
..Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease (C565928)
|
..Auditory Neuropathy, Nonsyndromic Recessive (C563398)
|
..Axenfeld-Rieger anomaly with cardiac defects and sensorineural hearing loss (C537789)
|
..Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities (C566234)
|
..BADS Syndrome (C562663)
|
..Barakat syndrome (C537907)
|
..Bartter Syndrome, Type 4A (C566530)
|
..Bartter Syndrome, Type 4b (C567762)
|
..Bjornstad syndrome (C537633)
|
..Boudhina Yedes Khiari syndrome (C537939)
|
..Brachydactyly, Intraventricular Septal Defect, And Deafness (C566521)
|
..Brown-Vialetto-Van Laere syndrome (C537111)
|
..CAPOS syndrome (C535351)
|
..Cardiomyopathy, Dilated, 1J (C565337)
|
..Cataract ataxia deafness (C538283)
|
..Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation (C563390)
|
..Cerebellar Ataxia and Hypergonadotropic Hypogonadism (C565308)
|
..Cerebellar Ataxia and Neurosensory Deafness (C565869)
|
..Cerebellar Ataxia, Deafness, and Narcolepsy (C565825)
|
..Charcot-Marie-Tooth disease and deafness (C538078)
|
..Charcot-Marie-Tooth disease, Type 2J (C535417)
|
..Chitty Hall Baraitser syndrome (C535928)
|
..Chudley-Mccullough syndrome (C535459)
|
..Cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss (C536427)
|
..Cochleosaccular degeneration of the inner ear and progressive cataracts (C536432)
|
..Coloboma, cleft lip/palate and mental retardation syndrome (C535971)
|
..Congenital ectodermal dysplasia with hearing loss (C535757)
|
..Corneal dystrophy and perceptive deafness (C535473)
|
..Cowchock syndrome (C536450)
|
..Craniofacial deafness hand syndrome (C536453)
|
..Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness (C565306)
|
..Deafness enamel hypoplasia nail defects (C535994)
|
..Deafness oligodontia syndrome (C538049)
|
..Deafness, Aminoglycoside-Induced (C564013)
|
..Deafness, Autosomal Dominant 1 (C565121)
|
..Deafness, Autosomal Dominant 10 (C563354)
|
..Deafness, Autosomal Dominant 11 (C563353)
|
..Deafness, Autosomal Dominant 12 (C563295)
|
..Deafness, Autosomal Dominant 13 (C566612)
|
..Deafness, Autosomal Dominant 15 (C566545)
|
..Deafness, Autosomal Dominant 16 (C565832)
|
..Deafness, Autosomal Dominant 18 (C565267)
|
..Deafness, Autosomal Dominant 20 (C565754)
|
..Deafness, Autosomal Dominant 21 (C564634)
|
..Deafness, Autosomal Dominant 23 (C565357)
|
..Deafness, Autosomal Dominant 24 (C565239)
|
..Deafness, Autosomal Dominant 25 (C565319)
|
..Deafness, Autosomal Dominant 28 (C563890)
|
..Deafness, Autosomal Dominant 2A (C567441)
|
..Deafness, Autosomal Dominant 2B (C567214)
|
..Deafness, Autosomal Dominant 30 (C564706)
|
..Deafness, Autosomal Dominant 31 (C563888)
|
..Deafness, Autosomal Dominant 36 (C564675)
|
..Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 (C565316)
|
..Deafness, Autosomal Dominant 3A (C567277)
|
..Deafness, Autosomal Dominant 3B (C567215)
|
..Deafness, Autosomal Dominant 4 (C563460)
|
..Deafness, Autosomal Dominant 41 (C564272)
|
..Deafness, Autosomal Dominant 43 (C564246)
|
..Deafness, Autosomal Dominant 44 (C564399)
|
..Deafness, Autosomal Dominant 47 (C563885)
|
..Deafness, Autosomal Dominant 48 (C564322)
|
..Deafness, Autosomal Dominant 49 (C564250)
|
..Deafness, Autosomal Dominant 5 (C563410)
|
..Deafness, Autosomal Dominant 52 (C564348)
|
..Deafness, Autosomal Dominant 53 (C566495)
|
..Deafness, Autosomal Dominant 59 (C567216)
|
..Deafness, Autosomal Dominant 6 (C563421)
|
..Deafness, Autosomal Dominant 7 (C563321)
|
..Deafness, Autosomal Dominant 9 (C563335)
|
..Deafness, autosomal dominant nonsyndromic sensorineural 17 (C538050)
|
..Deafness, autosomal dominant nonsyndromic sensorineural 22 (C538197)
|
..Deafness, autosomal dominant nonsyndromic sensorineural 23 (C538198)
|
..Deafness, autosomal dominant nonsyndromic sensorineural 24 (C538199)
|
..Deafness, Autosomal Recessive (C564609)
|
..Deafness, Autosomal Recessive 10 (C565341) 1
|
..Deafness, Autosomal Recessive 12 (C563327)
|
..Deafness, Autosomal Recessive 13 (C566410)
|
..Deafness, Autosomal Recessive 14 (C566344)
|
..Deafness, Autosomal Recessive 15 (C566611)
|
..Deafness, Autosomal Recessive 16 (C566339)
|
..Deafness, Autosomal Recessive 17 (C566418)
|
..Deafness, Autosomal Recessive 18 (C566580) 1
|
..Deafness, Autosomal Recessive 1A (C567134)
|
..Deafness, Autosomal Recessive 1b (C567213)
|
..Deafness, Autosomal Recessive 2 (C564007)
|
..Deafness, Autosomal Recessive 20 (C565828)
|
..Deafness, Autosomal Recessive 21 (C566353)
|
..Deafness, Autosomal Recessive 22 (C564633)
|
..Deafness, Autosomal Recessive 23 (C563705)
|
..Deafness, Autosomal Recessive 26 (C565329)
|
..Deafness, Autosomal Recessive 27 (C565287)
|
..Deafness, Autosomal Recessive 28 (C565218)
|
..Deafness, Autosomal Recessive 3 (C563961)
|
..Deafness, Autosomal Recessive 30 (C564624)
|
..Deafness, Autosomal Recessive 31 (C564629)
|
..Deafness, Autosomal Recessive 32 (C563884)
|
..Deafness, Autosomal Recessive 33 (C564602)
|
..Deafness, Autosomal Recessive 35 (C563908)
|
..Deafness, Autosomal Recessive 36 (C563815)
|
..Deafness, Autosomal Recessive 37 (C564331)
|
..Deafness, Autosomal Recessive 38 (C564273)
|
..Deafness, Autosomal Recessive 39 (C564265)
|
..Deafness, Autosomal Recessive 40 (C564266)
|
..Deafness, Autosomal Recessive 42 (C566460)
|
..Deafness, Autosomal Recessive 44 (C565716)
|
..Deafness, Autosomal Recessive 46 (C566459)
|
..Deafness, Autosomal Recessive 47 (C566498)
|
..Deafness, Autosomal Recessive 48 (C563720)
|
..Deafness, Autosomal Recessive 49 (C565717)
|
..Deafness, Autosomal Recessive 5 (C563444)
|
..Deafness, Autosomal Recessive 53 (C566453)
|
..Deafness, Autosomal Recessive 59 (C565698)
|
..Deafness, Autosomal Recessive 6 (C563418)
|
..Deafness, Autosomal Recessive 62 (C565719)
|
..Deafness, Autosomal Recessive 63 (C566951)
|
..Deafness, Autosomal Recessive 65 (C565211)
|
..Deafness, Autosomal Recessive 66 (C565701)
|
..Deafness, Autosomal Recessive 67 (C565207)
|
..Deafness, Autosomal Recessive 68 (C563669)
|
..Deafness, Autosomal Recessive 7 (C563417)
|
..Deafness, Autosomal Recessive 71 (C567562)
|
..Deafness, Autosomal Recessive 77 (C567543)
|
..Deafness, Autosomal Recessive 79 (C567651)
|
..Deafness, Autosomal Recessive 9 (C563396)
|
..Deafness, Autosomal Recessive, 24 (C567027)
|
..Deafness, Childhood-Onset Neurosensory, Autosomal Recessive 8 (C563395) 1
|
..Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia (C565195)
|
..Deafness, Congenital, with Total Albinism (C565646)
|
..Deafness, High-Frequency Sensorineural, X-Linked (C564432)
|
..Deafness, Mid-Tone Neural (C565122)
|
..Deafness, Progressive High-Tone Neural (C562423)
|
..Deafness, Sensorineural, And Male Infertility (C567010)
|
..Deafness, Sensorineural, Autosomal-Mitochondrial Type (C565637)
|
..Deafness, Sensorineural, with Hypertrophic Cardiomyopathy (C565236)
|
..Deafness, Sensorineural, with Peripheral Neuropathy and Arterial Disease (C565120)
|
..Deafness, X-Linked 1 (C564433)
|
..Deafness, X-Linked 3 (C564727)
|
..Deafness, X-Linked 4 (C564723)
|
..Deafness, X-Linked 5 (C564472)
|
..Digitorenocerebral Syndrome (C563052)
|
..Donnai-Barrow syndrome (C536390)
|
..Ectodermal Dysplasia and Neurosensory Deafness (C565606)
|
..Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features (C536182)
|
..Enlarged Vestibular Aqueduct (C566366)
|
..Ermine phenotype (C535508)
|
..Fitzsimmons Walson Mellor syndrome (C537937)
|
..Flynn Aird syndrome (C537066)
|
..Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness (C564999)
|
..Gemignani syndrome (C537678)
|
..Gonadal dysgenesis XX type deafness (C537286) 1
|
..Griscelli syndrome type 1 (C537301)
|
..Hearing Loss, Central (D006313) 16
|
..Hearing Loss, Noise-Induced (D006317)
|
..HID Syndrome (C566528)
|
..Histiocytosis with joint contractures and sensorineural deafness (C538322)
|
..Hittner Hirsch Kreh syndrome (C538323)
|
..Homozygous 11p15-p14 Deletion Syndrome (C564701)
|
..Insulin-Like Growth Factor I Deficiency (C563867)
|
..Johanson Blizzard syndrome (C535880)
|
..Keratoderma palmoplantar deafness (C536152)
|
..Knuckle pads, leuconychia and sensorineural deafness (C537210)
|
..Lipodystrophy, Generalized, with Mental Retardation, Deafness, Short Stature, and Slender Bones (C564283)
|
..Macrothrombocytopenia progressive deafness (C537831)
|
..Marshall syndrome (C536025)
|
..Martin-Probst Deafness-Mental Retardation Syndrome (C564495)
|
..MYH9-Related Disorders (C535507)
|
..Nephropathy deafness hyperparathyroidism (C536401)
|
..Nephropathy with Pretibial Epidermolysis Bullosa and Deafness (C563798)
|
..Nephropathy, Progressive, with Deafness (C563713)
|
..Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia (C566352)
|
..Nonsyndromic sensorineural hearing loss (C537845)
|
..Optic atrophy 1 and deafness (C537124)
|
..Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy (C565117)
|
..Otodental Dysplasia (C563482)
|
..Otofacioosseous-Gonadal Syndrome (C566597)
|
..OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA (OMIM:215150)
|
..Paragangliomas with Sensorineural Hearing Loss (C566831)
|
..Pendred syndrome (C536648)
|
..Pfeiffer Kapferer syndrome (C537887)
|
..Presbycusis (D011304) 2
|
..Progressive hearing loss stapes fixation (C536424)
|
..Prune Belly Syndrome with Pulmonic Stenosis, Mental Retardation, and Deafness (C562894)
|
..Renal Tubular Acidosis, Distal, Autosomal Recessive, with Late-Onset Sensorineural Hearing Loss (C566428)
|
..Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness (C562897)
|
..Retinitis Pigmentosa Inversa with Deafness (C564842)
|
..Robinson Miller Bensimon syndrome (C535864)
|
..Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction (C564829)
|
..Schaap Taylor Baraitser syndrome (C536626)
|
..Sensorineural Deafness With Mild Renal Dysfunction (C567544)
|
..Sensorineural Hearing Loss, Retinal Pigment Epithelium Lesions, Discolored Teeth (C566560)
|
..SeSAME syndrome (C557674)
|
..Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, And Progressive Nephropathy (C566682)
|
..Split-Hand/Foot Malformation With Sensorineural Hearing Loss (C565647)
|
..Spondyloepiphyseal Dysplasia, Myopia, And Sensorineural Deafness (C566659)
|
..Stickler Syndrome, Autosomal Recessive, COL9A1-Related (C565177)
|
..Stickler syndrome, type 1 (C537492)
|
..Thiamine responsive megaloblastic anemia syndrome (C536510)
|
..Townes-Brocks syndrome (C536974)
|
..Townes-Brocks-Branchiootorenal-Like Syndrome (C566272)
|
..Treft Sanborn Carey syndrome (C536544)
|
..Tunglang Savage Bellman syndrome (C536927)
|
..Usher Syndromes (D052245) 19
|
..Vohwinkel syndrome (C536457)
|
..Winkelman Bethge Pfeiffer syndrome (C536710)
|
..Wolfram Syndrome 2 (C565733)
|
..Wolfram Syndrome, Mitochondrial Form (C564012)
|
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
|