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Human Disease

autosomal recessive nonsyndromic deafness 88

Term ID
DOID:0110533
Synonyms
  • autosomal recessive deafness 88
  • DFNB88
Definition
An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the ELMOD3 gene on chromosome 2p11. https://www.ncbi.nlm.nih.gov/pubmed/24039609
References
Ontology
Human Disease   ( DOID:0110533 )
Relationships
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Genes Involved
Zebrafish Models