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Ontology Browser

Usher syndrome type 3B (DOID:0110842)
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 3A  
Usher syndrome type 3B  
An Usher syndrome type 3 that has_material_basis_in homozygous mutation in the HARS gene on chromosome 5q31. (DO)

Exact Synonyms: USH3B ;   Usher Syndrome, Type IIIB
Primary IDs: OMIM:614504
Alternate IDs: RDO:9000848
Definition Sources: "DO"

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