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aminoglycoside-induced deafness
Ataxia, Deafness, and Cardiomyopathy
ATAXIA, PROGRESSIVE SEIZURES, MENTAL DETERIORATION, AND HEARING LOSS
Athabaskan brainstem dysgenesis syndrome
autosomal dominant cerebellar ataxia, deafness and narcolepsy
autosomal dominant nonsyndromic deafness +
autosomal recessive nonsyndromic deafness +
autosomal recessive spinocerebellar ataxia 19
autosomal-mitochondrial sensorineural deafness
Axenfeld-Rieger Anomaly with Cardiac Defects and Sensorineural Hearing Loss
Boudhina Yedes Khiari syndrome
Brachydactyly, Intraventricular Septal Defect, and Deafness
BRANCHIAL ARCH ABNORMALITIES, CHOANAL ATRESIA, ATHELIA, HEARING LOSS, AND HYPOTHYROIDISM SYNDROME
Branchial Arch Syndrome X-Linked
Brown-Vialetto-Van Laere syndrome +
camptodactyly-tall stature-scoliosis-hearing loss syndrome
CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA
Cataracts, Hearing Impairment, Nephrotic Syndrome, and Enterocolitis +
Cerebellar Ataxia and Hypergonadotropic Hypogonadism
Cerebellar Ataxia and Neurosensory Deafness
Charcot-Marie-Tooth disease type 1E
Charcot-Marie-Tooth disease type 2J
Charcot-Marie-Tooth disease X-linked recessive 4
Chitty Hall Baraitser Syndrome
chromosome 6pter-p24 deletion syndrome
Chudley-Mccullough syndrome
CLEFT LIP AND PALATE-CRANIOFACIAL DYSMORPHISM-CONGENITAL HEART DEFECT-HEARING LOSS SYNDROME
Cleft Palate, Midfacial Hypoplasia, Triangular Facies, and Sensorineural Hearing Loss
Cochleosaccular Degeneration of the Inner Ear and Progressive Cataracts
Combined Cerebellar and Peripheral Ataxia with Hearing Loss and Diabetes Mellitus
combined pituitary hormone deficiency 3
Conductive Hearing Loss +
Cone-Rod Dystrophy and Hearing Loss +
Congenital Cataracts, Hearing Loss, and Neurodegeneration
Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia
Congenital Deafness with Total Albinism
Congenital Ectodermal Dysplasia with Hearing Loss
corneal dystrophy-perceptive deafness syndrome
craniofacial-deafness-hand syndrome
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness
Deafness, Congenital Heart Defects, and Posterior Embryotoxon
Deafness, Progressive High-Tone Neural
Deafness-Craniofacial Syndrome
Deafness-Infertility Syndrome
deafness-intellectual disability, Martin-Probst type syndrome
Deafness-Oligodontia Syndrome
Diabetes, Deafness, Developmental Delay, and Short Stature Syndrome
dilated cardiomyopathy 1J
distal arthrogryposis type 6
Distal Renal Tubular Acidosis 2 with Progressive Nerve Deafness
Distal Renal Tubular Acidosis 3, Autosomal Recessive
dominant optic atrophy plus syndrome
Ectodermal Dysplasia and Neurosensory Deafness
Ectodermal Dysplasia, Sensorineural Hearing Loss, and Distinctive Facial Features
Ehlers-Danlos syndrome kyphoscoliotic type 2
Epidermolysis Bullosa Simplex 7, with Nephropathy and Deafness
Familial Visceral Neuropathy 2, Autosomal Recessive
Fitzsimmons Walson Mellor Syndrome
Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness
Generalized Lipodystrophy with Mental Retardation, Deafness, Short Stature, and Slender Bones
Hearing Loss, Cisplatin-Induced
Hearing Loss, Mixed Conductive-Sensorineural +
Hearing Loss, Noise-Induced
Hearing Loss, Unilateral Sensorineural
high myopia-sensorineural deafness syndrome
High-Frequency Hearing Loss + Hearing loss in frequencies above 1000 hertz.
histiocytosis-lymphadenopathy plus syndrome
Hittner Hirsch Kreh Syndrome
Homozygous 11p15-p14 Deletion Syndrome
hypoparathyroidism-deafness-renal disease syndrome
Insulin-Like Growth Factor I Deficiency
Iris Dysplasia Hypertelorism Deafness
Johanson-Blizzard syndrome
Keratoderma-Ichthyosis-Deafness Syndrome, Autosomal Recessive
Microcephaly, Growth Retardation, Cataract, Hearing Loss, and Unusual Appearance
Microtia, Hearing Impairment, and Cleft Palate
midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis
Mitochondrial Progressive Myopathy with Congenital Cataract, Hearing Loss, and Developmental Delay
MUSCULAR DYSTROPHY, CONGENITAL HEARING LOSS, AND OVARIAN INSUFFICIENCY SYNDROME
Nephropathy, Deafness, and Hyperparathyroidism
NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS AND SPASTICITY
neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities
neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss
Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia
Nonsyndromic Sensorineural Hearing Loss +
ocular albinism with sensorineural deafness
Odontochondrodysplasia 2 with Hearing Loss and Diabetes
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant
Osteootohepatoenteric Syndrome
Otofacioosseous-Gonadal Syndrome
otospondylomegaepiphyseal dysplasia, autosomal recessive
palmoplantar keratoderma-deafness syndrome
Paragangliomas with Sensorineural Hearing Loss
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss
Pfeiffer Kapferer Syndrome
Pigmentary Retinopathy and Sensorineural Deafness
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease
Progressive Nephropathy with Deafness
Prune Belly Syndrome with Pulmonic Stenosis, Mental Retardation, and Deafness
Reardon Wilson Cavanagh Syndrome
Retinitis Pigmentosa Inversa with Deafness
Robinson Miller Bensimon Syndrome
Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction
Schaap Taylor Baraitser Syndrome
Sensorineural Deafness and Migraine
Sensorineural Deafness with Hypertrophic Cardiomyopathy
Sensorineural Deafness with Mild Renal Dysfunction
Sensorineural Deafness with Peripheral Neuropathy and Arterial Disease
sensorineural hearing loss +
Sensorineural Hearing Loss, Retinal Pigment Epithelium Lesions, Discolored Teeth
short stature, hearing loss, retinitis pigmentosa, and distinctive facies
Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy
split hand-foot malformation 1 with sensorineural hearing loss
Spondyloepiphyseal Dysplasia, Myopia, and Sensorineural Deafness
spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis
Spondylomegaepiphyseal Dysplasia with Upper Limb Mesomelia, Punctate Calcifications, and Deafness
syndromic X-linked intellectual disability Abidi type
thiamine-responsive megaloblastic anemia syndrome
Treft Sanborn Carey Syndrome
Tunglang Savage Bellman Syndrome
Unilateral Hearing Loss +
uveal coloboma-cleft lip and palate-intellectual disability
Wolfram syndrome, mitochondrial form
X-linked nonsyndromic deafness +
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