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Human Disease

autosomal recessive nonsyndromic deafness 36

Term ID
DOID:0110494
Synonyms
  • autosomal recessive deafness 36
  • DFNB36
Definition
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the ESPN gene on chromosome 1p36. https://www.ncbi.nlm.nih.gov/pubmed/15286153
References
Ontology
Human Disease   ( DOID:0110494 )
Relationships
is a type of
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Genes Involved
Zebrafish Models