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aminoglycoside-induced deafness
anterior segment dysgenesis 4
Ataxia, Deafness, and Cardiomyopathy
Athabaskan brainstem dysgenesis syndrome
Auditory Neuropathy, Nonsyndromic Recessive
autosomal dominant cerebellar ataxia, deafness and narcolepsy
autosomal dominant congenital deafness with onychodystrophy
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
blepharocheilodontic syndrome +
Boudhina Yedes Khiari syndrome
Brachydactyly, Intraventricular Septal Defect, and Deafness
Brown-Vialetto-Van Laere syndrome +
Carabelli Anomaly of Maxillary Molar Teeth
CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA
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
Chudley-Mccullough syndrome
Cleft Palate, Midfacial Hypoplasia, Triangular Facies, and Sensorineural Hearing Loss
Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only
Cochleosaccular Degeneration of the Inner Ear and Progressive Cataracts
Combined Pituitary Hormone Deficiency, 3
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
Craniosynostosis and Dental Anomalies
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness
Deafness, Progressive High-Tone Neural
deafness-intellectual disability, Martin-Probst type syndrome
Deafness-Oligodontia Syndrome
dental enamel hypoplasia +
dentinogenesis imperfecta +
DEVELOPMENTAL DELAY WITH DYSMORPHIC FACIES AND DENTAL ANOMALIES
Diabetes, Deafness, Developmental Delay, and Short Stature Syndrome
Diamond-Blackfan Anemia with Microtia and Cleft Palate
dilated cardiomyopathy 1J
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis
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
Epidermolysis Bullosa Simplex 7, with Nephropathy and Deafness
Euhidrotic Ectodermal Dysplasia
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
Grubben de Cock Borghgraef Syndrome
Hearing Loss, Cisplatin-Induced
Hearing Loss, Noise-Induced
Hearing Loss, Unilateral Sensorineural
high myopia-sensorineural deafness syndrome
High-Frequency Hearing Loss +
histiocytosis-lymphadenopathy plus syndrome
Hittner Hirsch Kreh Syndrome
Homozygous 11p15-p14 Deletion Syndrome
hypertelorism, microtia, facial clefting syndrome
hypoparathyroidism-deafness-renal disease syndrome
HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME
Insulin-Like Growth Factor I Deficiency
Isotretinoin Embryopathy Like Syndrome
Johanson-Blizzard syndrome
Keratoderma-Ichthyosis-Deafness Syndrome, Autosomal Recessive
Lethal Faciocardiomelic Dysplasia
Mastocytosis, Cutaneous, with Short Stature, Conductive Hearing Loss and Microtia
Microtia with Nasolacrimal Duct Imperforation and Eye Coloboma
Microtia, Hearing Impairment, and Cleft Palate
Microtia, Meatal Atresia and Conductive Deafness
MUSCULAR DYSTROPHY, CONGENITAL HEARING LOSS, AND OVARIAN INSUFFICIENCY SYNDROME
Nephropathy, Deafness, and Hyperparathyroidism
Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia
Noneruption of Teeth with Maxillary Hypoplasia and Genu Valgum
Nonsyndromic Sensorineural Hearing Loss +
ocular albinism with sensorineural deafness
oculodentodigital dysplasia +
Oculoskeletodental Syndrome
Odontomicronychial Dysplasia
Odontotrichoungual-Digital-Palmar Syndrome
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy
Oroacral Syndrome, Verloes-Koulischer Type
Otofacioosseous-Gonadal Syndrome
otospondylomegaepiphyseal dysplasia, autosomal recessive
palmoplantar keratoderma-deafness syndrome
Paragangliomas with Sensorineural Hearing Loss
Pfeiffer Kapferer Syndrome
Pigmentary Retinopathy and Sensorineural Deafness
Postaxial Polydactyly, with Dental and Vertebral Anomalies
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
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 Male Infertility
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, Retinal Pigment Epithelium Lesions, Discolored Teeth
Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy
split hand-foot malformation 1 with sensorineural hearing loss
Spondyloepimetaphyseal Dysplasia with Abnormal Dentition
Spondyloepiphyseal Dysplasia, Myopia, and Sensorineural Deafness
spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis
Taurodontism, Microdontia, and Dens Invaginatus
temtamy preaxial brachydactyly syndrome
thiamine-responsive megaloblastic anemia syndrome
Treft Sanborn Carey Syndrome
Tricho-Dento-Osseous Syndrome 1
Tunglang Savage Bellman Syndrome
uveal coloboma-cleft lip and palate-intellectual disability
Weyers acrofacial dysostosis
Wolfram syndrome, mitochondrial form
X-linked nonsyndromic deafness +
Zazam Sheriff Phillips Syndrome
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