OBO ID: DOID:0111736
Term Name: X-linked deafness 3 Search Ontology:
Synonyms:
  • congenital sensorineural X-linked deafness 4
  • DFN4
  • DFNX3
Definition: An X-linked nonsyndromic deafness characterized by congenital, bilateral, profound and sensorineural hearing loss in males and bilateral, mild to moderate high frequency sensorineural hearing impairment with later onset in heterozygous females that has_material_basis_in mutation in a region on chromosome Xp21.2. (2)
References:
Ontology: Human Disease   ( DOID:0111736 )
Relationships
is a type of:
OTHER X-linked deafness 3 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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.