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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Usher syndrome +     
retinitis pigmentosa-deafness syndrome  
Usher syndrome type 1 +   
Autosomal recessive hereditary disorders characterized by congenital SENSORINEURAL HEARING LOSS and RETINITIS PIGMENTOSA. Subtypes include types 1B - 1I.
Usher syndrome type 2 +   
Usher syndrome type 3 +   
Usher Syndrome Type 4  

Synonyms
Exact Synonyms: US1 ;   USH1 ;   Usher Syndrome, Type I
Primary IDs: RDO:9000055
Xrefs: NCI:C126327 ;   ORDO:231169
Definition Sources: https://ghr.nlm.nih.gov/condition/usher-syndrome "DO", https://www.ncbi.nlm.nih.gov/books/NBK1265/ "DO", https://www.ncbi.nlm.nih.gov/pubmed/2909824 "DO"

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.