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3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
Absence of Tibia with Congenital Deafness
Albinism Deafness Syndrome
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death
autosomal dominant congenital deafness with onychodystrophy
autosomal dominant nonsyndromic deafness 65
Branchiogenic-Deafness Syndrome
Cardioauditory Syndrome of Sanchez Cascos
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS
Congenital Deafness and Familial Myoclonic Epilepsy
Congenital Deafness, with Vitiligo and Achalasia
Congenital Emphysema, with Deafness, Penoscrotal Web, and Mental Retardation
Congenital Myopathy with Neuropathy and Deafness
Davenport Donlan Syndrome
Deafness Hyperuricemia Neurologic Ataxia
Deafness with Anhidrotic Ectodermal Dysplasia
Deafness, Autosomal Dominant, due to Mutation In Myo1a
DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities
Deafness, Congenital Onychodystrophy, Recessive Form
DEAFNESS, CONGENITAL, AND ADULT-ONSET PROGRESSIVE LEUKOENCEPHALOPATHY
Deafness, with Smith-Magenis Syndrome
Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation
Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness
hereditary spastic paraplegia 24
high myopia-sensorineural deafness syndrome
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness
Hyperlipoproteinemia Type II, and Deafness
HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS
Hypokalemic Tubulopathy and Deafness
ITM2B-related cerebral amyloid angiopathy 2
Johnson Neuroectodermal Syndrome
Keratitis-Ichthyosis-Deafness Syndrome +
Konigsmark Knox Hussels Syndrome
LEUKOENCEPHALOPATHY, PROGRESSIVE, INFANTILE-ONSET, WITH OR WITHOUT DEAFNESS
Lynch Lee Murday syndrome
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome
Meyenburg-Altherr-Uehlinger Syndrome
Microcephaly Deafness Syndrome
multiple synostoses syndrome 1
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders
Myoclonus, Cerebellar Ataxia, and Deafness
Nephrosis with Deafness and Urinary Tract and Digital Malformations
Noninsulin-Dependent Diabetes Mellitus with Deafness
nonsyndromic deafness + An auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms. (DO)
Opticocochleodentate Degeneration
Ramos Arroyo Clark Syndrome
Ribbonlike Corneal Degeneration with Deafness
Schimke X-Linked Mental Retardation Syndrome
Schlegelberger Grote Syndrome
Secretory Diarrhea, Myopathy, and Deafness
Sinoatrial Node Dysfunction and Deafness
spastic paraplegia with deafness
temtamy preaxial brachydactyly syndrome
X-linked mental retardation Gustavson type
X-linked mental retardation-hypotonic facies syndrome-1
X-linked retinitis pigmentosa and sinorespiratory infections
Yemenite Deaf-Blind Hypopigmentation Syndrome
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