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Ontology Browser

Term:
autosomal dominant nonsyndromic deafness 65 (DOID:0110586)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2) Pig: (2) Naked Mole-rat: (2) Green Monkey: (2)
Parent Terms Term With Siblings Child Terms
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 auditory neuropathy 1  
Autosomal Dominant Auditory Neuropathy 2  
autosomal dominant auditory neuropathy 3  
autosomal dominant congenital deafness with onychodystrophy  
Autosomal Dominant Deafness 39 with Dentinogenesis Imperfecta 1  
Autosomal Dominant Deafness 4  
autosomal dominant nonsyndromic deafness 1  
autosomal dominant nonsyndromic deafness 10  
autosomal dominant nonsyndromic deafness 11  
autosomal dominant nonsyndromic deafness 12  
autosomal dominant nonsyndromic deafness 13  
autosomal dominant nonsyndromic deafness 15  
autosomal dominant nonsyndromic deafness 16  
autosomal dominant nonsyndromic deafness 17  
autosomal dominant nonsyndromic deafness 18 
autosomal dominant nonsyndromic deafness 20  
autosomal dominant nonsyndromic deafness 21  
autosomal dominant nonsyndromic deafness 22  
autosomal dominant nonsyndromic deafness 23  
autosomal dominant nonsyndromic deafness 24 
autosomal dominant nonsyndromic deafness 25  
autosomal dominant nonsyndromic deafness 27  
autosomal dominant nonsyndromic deafness 28  
autosomal dominant nonsyndromic deafness 2A  
autosomal dominant nonsyndromic deafness 2B  
autosomal dominant nonsyndromic deafness 30  
autosomal dominant nonsyndromic deafness 31 
autosomal dominant nonsyndromic deafness 33  
autosomal dominant nonsyndromic deafness 34  
autosomal dominant nonsyndromic deafness 36  
Autosomal Dominant Nonsyndromic Deafness 37  
autosomal dominant nonsyndromic deafness 3A  
autosomal dominant nonsyndromic deafness 3B  
autosomal dominant nonsyndromic deafness 40  
autosomal dominant nonsyndromic deafness 41  
autosomal dominant nonsyndromic deafness 43 
autosomal dominant nonsyndromic deafness 44  
autosomal dominant nonsyndromic deafness 47 
autosomal dominant nonsyndromic deafness 48  
autosomal dominant nonsyndromic deafness 49 
autosomal dominant nonsyndromic deafness 4A  
autosomal dominant nonsyndromic deafness 4B  
autosomal dominant nonsyndromic deafness 5  
autosomal dominant nonsyndromic deafness 50  
autosomal dominant nonsyndromic deafness 51  
autosomal dominant nonsyndromic deafness 52 
autosomal dominant nonsyndromic deafness 53 
autosomal dominant nonsyndromic deafness 54 
autosomal dominant nonsyndromic deafness 56  
autosomal dominant nonsyndromic deafness 58  
autosomal dominant nonsyndromic deafness 59 
autosomal dominant nonsyndromic deafness 6  
autosomal dominant nonsyndromic deafness 64  
autosomal dominant nonsyndromic deafness 65  
An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the TBC1D24 gene on chromosome 16p13. (DO)
autosomal dominant nonsyndromic deafness 66  
autosomal dominant nonsyndromic deafness 67  
autosomal dominant nonsyndromic deafness 68  
autosomal dominant nonsyndromic deafness 69  
autosomal dominant nonsyndromic deafness 7  
autosomal dominant nonsyndromic deafness 70  
autosomal dominant nonsyndromic deafness 71  
autosomal dominant nonsyndromic deafness 72  
autosomal dominant nonsyndromic deafness 73  
autosomal dominant nonsyndromic deafness 74  
autosomal dominant nonsyndromic deafness 75  
autosomal dominant nonsyndromic deafness 76  
autosomal dominant nonsyndromic deafness 77  
autosomal dominant nonsyndromic deafness 78  
autosomal dominant nonsyndromic deafness 79  
Autosomal Dominant Nonsyndromic Deafness 80  
Autosomal Dominant Nonsyndromic Deafness 81  
Autosomal Dominant Nonsyndromic Deafness 82  
Autosomal Dominant Nonsyndromic Deafness 83  
Autosomal Dominant Nonsyndromic Deafness 84  
Autosomal Dominant Nonsyndromic Deafness 85  
Autosomal Dominant Nonsyndromic Deafness 86  
Autosomal Dominant Nonsyndromic Deafness 87  
Autosomal Dominant Nonsyndromic Deafness 88  
Autosomal Dominant Nonsyndromic Deafness 89  
autosomal dominant nonsyndromic deafness 9  
Autosomal Dominant Nonsyndromic Deafness 90  
Ayazi Syndrome 
Branchiogenic-Deafness Syndrome 
Burn-McKeown 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  
Coxoauricular Syndrome 
Davenport Donlan Syndrome 
Deaf-Blind Disorders +   
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 
Fine-Lubinsky Syndrome  
Fountain Syndrome 
hereditary spastic paraplegia 24 
Herrmann Syndrome 
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 
Jones Syndrome 
Keipert 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 
Muckle-Wells syndrome  
multiple synostoses syndrome 1  
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders 
Myoclonus, Cerebellar Ataxia, and Deafness 
Nathalie Syndrome 
Nephrosis with Deafness and Urinary Tract and Digital Malformations 
Noninsulin-Dependent Diabetes Mellitus with Deafness  
nonsyndromic deafness +   
Opticocochleodentate Degeneration 
Perrault syndrome +   
Ramos Arroyo Clark Syndrome 
Ribbonlike Corneal Degeneration with Deafness 
Richards-Rundle Syndrome 
Schimke X-Linked Mental Retardation Syndrome 
Schlegelberger Grote Syndrome 
Secretory Diarrhea, Myopathy, and Deafness 
Siddiqi syndrome  
Sinoatrial Node Dysfunction and Deafness  
spastic paraplegia with deafness 
temtamy preaxial brachydactyly syndrome  
Tietz syndrome  
Wright Dyck Syndrome 
X-linked Alport 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 

Synonyms
Related Synonyms: DFNA65 ;   autosomal dominant deafness 65
Primary IDs: MIM:616044 ;   RDO:9002446
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/24729539 "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/24729547 "DO" "DO"

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