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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Hearing Loss +     
ATAXIA, PROGRESSIVE SEIZURES, MENTAL DETERIORATION, AND HEARING LOSS  
Behr syndrome  
Bilateral Hearing Loss +   
BRANCHIAL ARCH ABNORMALITIES, CHOANAL ATRESIA, ATHELIA, HEARING LOSS, AND HYPOTHYROIDISM SYNDROME  
Branchial Arch Syndrome X-Linked 
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
Cataracts, Hearing Impairment, Nephrotic Syndrome, and Enterocolitis +   
chromosome 6pter-p24 deletion syndrome 
Combined Cerebellar and Peripheral Ataxia with Hearing Loss and Diabetes Mellitus  
Conductive Hearing Loss +   
Hearing loss due to interference with the mechanical reception or amplification of sound to the COCHLEA. The interference is in the outer or middle ear involving the EAR CANAL; TYMPANIC MEMBRANE; or EAR OSSICLES.
Cone-Rod Dystrophy and Hearing Loss +   
Congenital Cataracts, Hearing Loss, and Neurodegeneration  
Deafness +   
Deafness, Congenital Heart Defects, and Posterior Embryotoxon  
Deafness-Craniofacial Syndrome 
Ehlers-Danlos syndrome kyphoscoliotic type 2  
Functional Hearing Loss 
Hearing Loss, Mixed Conductive-Sensorineural +  
High-Frequency Hearing Loss +   
Iris Dysplasia Hypertelorism Deafness 
LADD syndrome +   
Microcephaly, Growth Retardation, Cataract, Hearing Loss, and Unusual Appearance 
Microtia, Hearing Impairment, and Cleft Palate  
midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis  
Mitchell syndrome  
Mitochondrial Progressive Myopathy with Congenital Cataract, Hearing Loss, and Developmental Delay  
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  
Odontochondrodysplasia 2 with Hearing Loss and Diabetes  
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant 
Osteootohepatoenteric Syndrome  
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
Reardon Wilson Cavanagh Syndrome 
sensorineural hearing loss +   
short stature, hearing loss, retinitis pigmentosa, and distinctive facies  
Spondylomegaepiphyseal Dysplasia with Upper Limb Mesomelia, Punctate Calcifications, and Deafness 
syndromic X-linked intellectual disability Abidi type 
Unilateral Hearing Loss +   
uveal coloboma-cleft lip and palate-intellectual disability  

Synonyms
Primary IDs: MESH:D006314
Alternate IDs: RDO:0000754
Definition Sources: MESH:D006314

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