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Ontology Browser

Term:
autosomal dominant nonsyndromic deafness 17 (DOID:0110548)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
autosomal dominant auditory neuropathy 1  
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  
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the MYH9 gene on chromosome 22q12. (DO)
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  
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 9  

Synonyms
Exact Synonyms: DFNA17 ;   Late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration ;   autosomal dominant deafness 17 ;   deafness, autosomal dominant nonsyndromic sensorineural 17
Narrow Synonyms: COCHLEOSACCULAR DEGENERATION
Primary IDs: MESH:C538050
Alternate IDs: OMIM:603622 ;   RDO:0003984
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/11023810 "DO"

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