Search Ontology:
Human Disease

Usher syndrome type 2

Term ID
DOID:0110827
Synonyms
  • USH2
Definition
An Usher syndrome characterized by mild to severe congenital hearing impairment, normal vestibular function and later development of retinitis pigmentosa. (4)
References
  • MESH:D052245
  • NCI:C126328
  • ORDO:231178
  • SNOMEDCT_US_2021_09_01:232058008
Ontology
Human Disease   ( DOID:0110827 )
Relationships
is a type of
has subtype
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.