OBO ID: DOID:0110592
Term Name: autosomal dominant nonsyndromic deafness 70 Search Ontology:
Synonyms:
  • autosomal dominant deafness 70
  • DFNA70
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the MCM2 gene on chromosome 3q21. https://www.ncbi.nlm.nih.gov/pubmed/26196677
References:
Ontology: Human Disease   ( DOID:0110592 )
Relationships
is a type of:
OTHER autosomal dominant nonsyndromic deafness 70 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MCM2 ?Deafness, autosomal dominant 70 616968
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.