Search Ontology:
Human Disease

autosomal recessive nonsyndromic deafness 25

Term ID
DOID:0110483
Synonyms
  • autosomal recessive deafness 25
  • DFNB25
Definition
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, progressive hearing loss and has_material_basis_in mutation in the GRXCR1 gene on chromosome 4p13. https://www.ncbi.nlm.nih.gov/pubmed/20137778
References
Ontology
Human Disease   ( DOID:0110483 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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