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Ontology Browser

Term:
Usher syndrome type 1G (DOID:0110834)
Annotations: Rat: (3) Mouse: (3) Human: (3) Chinchilla: (3) Bonobo: (3) Dog: (3) Squirrel: (3) Pig: (3)
Parent Terms Term With Siblings Child Terms
Usher Syndrome Type 1B  
Usher syndrome type 1C  
Usher syndrome type 1D +   
Usher syndrome type 1E 
Usher syndrome type 1F +   
Usher syndrome type 1G  
An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25. (DO)
Usher syndrome type 1H 
Usher syndrome type 1J  
Usher syndrome type 1K 
Usher Syndrome Type 1M  

Synonyms
Exact Synonyms: USH1G ;   USH1G-RELATED DISORDER ;   USH1G-RELATED DISORDERS ;   Usher syndrome type IG
Primary IDs: MESH:C564643 ;   RDO:0011956
Alternate IDs: OMIM:606943
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/12588794 "DO"

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