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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Usher Syndrome Type 1B  
Usher syndrome type 1C  
An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15. (DO)
Usher syndrome type 1D +   
Usher syndrome type 1E 
Usher syndrome type 1F +   
Usher syndrome type 1G  
Usher syndrome type 1H 
Usher syndrome type 1J  
Usher syndrome type 1K 
Usher Syndrome Type 1M  

Synonyms
Exact Synonyms: USH1C ;   Usher syndrome type I Acadian variety ;   Usher syndrome type IC ;   Usher syndrome, Acadian variety
Primary IDs: MESH:C536486 ;   MESH:C564753
Alternate IDs: OMIM:276904
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/10973247 "DO" "DO"

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