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Ontology Browser
Term:
Ribbonlike Corneal Degeneration with Deafness (DOID:9001950)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0) Naked Mole-rat: (0) Green Monkey: (0)
Parent Terms Term With Siblings Child Terms
corneal dystrophy +     
Deafness +     
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome  
Absence of Tibia with Congenital Deafness 
Albinism Deafness Syndrome 
aniridia 1  
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death 
autosomal dominant congenital deafness with onychodystrophy  
autosomal dominant nonsyndromic deafness 65  
Ayazi Syndrome 
band keratopathy 
Bietti crystalline corneoretinal dystrophy  
Brachymesomelia Renal Syndrome 
Branchiogenic-Deafness Syndrome 
Burn-McKeown syndrome  
Cardioauditory Syndrome of Sanchez Cascos 
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS  
Congenital Corneal Opacities, Cornea Guttata, and Corectopia 
Congenital Deafness and Familial Myoclonic Epilepsy 
Congenital Deafness, with Vitiligo and Achalasia 
Congenital Emphysema, with Deafness, Penoscrotal Web, and Mental Retardation 
Congenital Hereditary Endothelial Dystrophy with Nail Hypoplasia 
Congenital Myopathy with Neuropathy and Deafness  
Corneal Cerebellar Syndrome 
corneal dystrophy-perceptive deafness syndrome  
corneal endothelial dystrophy +   
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  
Dermochondrocorneal Dystrophy of François 
Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation 
EDICT Syndrome  
Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness 
epithelial and subepithelial dystrophy +   
epithelial-stromal TGFBI dystrophy +   
Fine-Lubinsky Syndrome  
Fountain Syndrome 
foveal hypoplasia 1  
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  
Ichthyosiform Erythroderma, Corneal Involvement, Deafness  
ITM2B-related cerebral amyloid angiopathy 2  
Johnson Neuroectodermal Syndrome 
Jones Syndrome 
Judge Misch Wright Syndrome 
Keipert syndrome  
Keratitis-Ichthyosis-Deafness Syndrome +   
Konigsmark Knox Hussels Syndrome 
Kuster Majewski Hammerstein 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 
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus  
Mousa Al din Al Nassar 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 +   
Oculodental Syndrome Rutherfurd Syndrome 
Opticocochleodentate Degeneration 
Perrault syndrome +   
posterior polymorphous corneal dystrophy +   
Progressive Bifocal Chorioretinal Atrophy  
Ramos Arroyo Clark Syndrome 
Reis-Bucklers corneal dystrophy  
Ribbonlike Corneal Degeneration with Deafness 
Richards-Rundle Syndrome 
Sammartino De Crecchio 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 
spondyloepiphyseal dysplasia with punctate corneal dystrophy 
spondylometaphyseal dysplasia with corneal dystrophy  
stromal dystrophy +   
Sveinsson chorioretinal atrophy  
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
Exact Synonyms: Band Keratopathy with Deafness
Primary IDs: MESH:C565157
Alternate IDs: MIM:121450

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