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Ontology Browser

Term:
Usher syndrome type 2D (DOID:0110840)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Usher syndrome type 2A  
Usher syndrome type 2C  
Usher syndrome type 2D  
An Usher syndrome type 2 that has_material_basis_in by homozygous or compound heterozygous mutation in the WHRN gene on chromosome 9q32. (DO)
Usher Syndrome, Type 2B  

Synonyms
Exact Synonyms: USH2D ;   Usher Syndrome, Type IID
Primary IDs: OMIM:611383 ;   RDO:0009522
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/17171570 "DO"

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