Search Ontology:
Human Disease

Usher syndrome type 1G

Term ID
DOID:0110834
Synonyms
  • USH1G
  • Usher syndrome type IG
Definition
An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25. https://www.ncbi.nlm.nih.gov/pubmed/12588794
References
Ontology
Human Disease   ( DOID:0110834 )
Relationships
is a type of
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.