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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
cone-rod dystrophy +     
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 
CLEFT LIP AND PALATE-CRANIOFACIAL DYSMORPHISM-CONGENITAL HEART DEFECT-HEARING LOSS SYNDROME  
Combined Cerebellar and Peripheral Ataxia with Hearing Loss and Diabetes Mellitus  
Conductive Hearing Loss +   
cone-rod dystrophy 1  
cone-rod dystrophy 10  
cone-rod dystrophy 11  
cone-rod dystrophy 12  
cone-rod dystrophy 13  
cone-rod dystrophy 14  
cone-rod dystrophy 15  
cone-rod dystrophy 16  
cone-rod dystrophy 17 
cone-rod dystrophy 18  
cone-rod dystrophy 19  
cone-rod dystrophy 2  
cone-rod dystrophy 20  
cone-rod dystrophy 21  
cone-rod dystrophy 22  
cone-rod dystrophy 24  
cone-rod dystrophy 3  
cone-rod dystrophy 5  
cone-rod dystrophy 6  
cone-rod dystrophy 7  
cone-rod dystrophy 8 
cone-rod dystrophy 9  
Cone-Rod Dystrophy and Hearing Loss +   
CONE-ROD SYNAPTIC DISORDER SYNDROME, CONGENITAL NONPROGRESSIVE  
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 
Microcornea, Rod-Cone Dystrophy, Cataract, and Posterior Staphyloma 1  
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  
Newfoundland cone-rod dystrophy  
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 
Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction  
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  
X-linked cone-rod dystrophy 1  
X-linked cone-rod dystrophy 2 
X-linked cone-rod dystrophy 3  

Synonyms
Exact Synonyms: CRDHL
Xrefs: EFO:0009151 ;   MIM:PS617236

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