OBO ID: DOID:0110557
Term Name: autosomal dominant nonsyndromic deafness 28 Search Ontology:
Synonyms:
  • autosomal dominant deafness 28
  • DFNA28
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has_material_basis_in mutation in the GRHL2 gene on chromosome 8q22. https://www.ncbi.nlm.nih.gov/pubmed/12393799
References:
Ontology: Human Disease   ( DOID:0110557 )
Relationships
is a type of:
OTHER autosomal dominant nonsyndromic deafness 28 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GRHL2 Deafness, autosomal dominant 28 608641
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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